NDC Product
Human Prescription DrugNorvir NDC 0074-3399
- Generic Name
- Ritonavir
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Anhydrous Citric Acid, uniquely identified by the FDA Unique Ingredient Identifier (UNII) XF417D3PSL.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 77-92-9 and the RxNorm Concept ID (RxCUI) 221946. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
ANHYDROUS CITRIC ACID
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
XF417D3PSL
The specific atomic composition represented as a molecular structure string.
InChIKey
C6H8O7 International Chemical Identifier digital signature for unique molecular identification.
SMILES String
KRKNYBCHXYNGOX-UHFFFAOYSA-N Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
C(CC(=O)O)(CC(=O)O)(C(=O)O)O
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Anhydrous Citric Acid. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.
Common Names & Synonyms
1,2,3-PROPANETRICARBOXYLIC ACID, 2-HYDROXY-
CN
ACIDUM CITRICUM [WHO-IP LATIN]
CN
ACILETTEN
CN
ANHYDROUS CITRIC ACID
CN
ANHYDROUS CITRIC ACID [II]
CN
ANHYDROUS CITRIC ACID [JAN]
CN
ANHYDROUS CITRIC ACID [MART.]
CN
ANHYDROUS CITRIC ACID [USP MONOGRAPH]
CN
CITRIC ACID (CONSTITUENT OF CRANBERRY LIQUID PREPARATION) [DSC]
CN
CITRIC ACID (CONSTITUENT OF GARCINIA CAMBOGIA AND GARCINIA INDICA) [DSC]
CN
CITRIC ACID [FHFI]
CN
CITRIC ACID [HSDB]
CN
CITRIC ACID [MI]
CN
CITRIC ACID [WHO-DD]
CN
CITRIC ACID ANHYDROUS
CN
CITRIC ACID MONOGLYCERIDE
CN
CITRIC ACID, ANHYDROUS
CN
CITRIC ACID, ANHYDROUS [EP IMPURITY]
CN
CITRIC ACID, ANHYDROUS [USP IMPURITY]
CN
CITRIC ACID, ANHYDROUS [WHO-IP]
CN
CITRIC ACID,ANHYDROUS
CN
CITRIC ACID,ANHYDROUS [VANDF]
CN
CITRICUM ACIDUM
CN
CITRICUM ACIDUM [HPUS]
CN
Brand / Trade Names
CLENPIQ COMPONENT ANHYDROUS CITRIC ACID
BN
Systematic Nomenclature
2-HYDROXY-1,2,3-PROPANETRICARBOXYIC ACID
SYS
3-CARBOXY-3-HYDROXYPENTANE-1,5-DIOIC ACID
SYS
Technical Codes
FEMA NO. 2306
CD
NSC-112226
CD
NSC-30279
CD
NSC-626579
CD
NDC Products Containing ANHYDROUS CITRIC ACID
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:
Manufacturer Quick Index
Note: Due to the high number of listings (500), only Active Listings are currently displayed. Display is limited to the first 200 products.
Showing 200 active products
AbbVie Inc.
Active Listing
Alcon Laboratories, Inc.
NDC Product
Human Prescription DrugInveltys NDC 0065-9307
- Generic Name
- Loteprednol Etabonate
- Dosage Form
- Suspension
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugChloroquine Phosphate NDC 0115-7010
- Generic Name
- Chloroquine Phosphate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
AstraZeneca Pharmaceuticals LP
NDC Product
Human Prescription DrugPulmicort Respules NDC 0186-1988
- Generic Name
- Budesonide
- Dosage Form
- Suspension
- Route
- Respiratory (inhalation)
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPulmicort Respules NDC 0186-1989
- Generic Name
- Budesonide
- Dosage Form
- Suspension
- Route
- Respiratory (inhalation)
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPulmicort Respules NDC 0186-1990
- Generic Name
- Budesonide
- Dosage Form
- Suspension
- Route
- Respiratory (inhalation)
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4010
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4020
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4025
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
C.B. Fleet Company, Inc.
NDC Product
Human Otc DrugBoudreauxs NDC 0132-0334
- Generic Name
- Zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
NDC Product
Human Prescription DrugClobetasol Propionate NDC 0168-0163
- Generic Name
- Clobetasol Propionate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClobetasol Propionate NDC 0168-0293
- Generic Name
- Clobetasol Propionate
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
Eli Lilly and Company
NDC Product
Human Prescription DrugTrulicity NDC 0002-1433
- Generic Name
- Dulaglutide
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugTrulicity NDC 0002-1434
- Generic Name
- Dulaglutide
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugTaltz NDC 0002-1445
- Generic Name
- Ixekizumab
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugTrulicity NDC 0002-2236
- Generic Name
- Dulaglutide
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugTrulicity NDC 0002-3182
- Generic Name
- Dulaglutide
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugOmvoh NDC 0002-7575
- Generic Name
- Mirikizumab-mrkz
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugTaltz NDC 0002-7724
- Generic Name
- Ixekizumab
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugOmvoh NDC 0002-8011
- Generic Name
- Mirikizumab-mrkz
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugKisunla NDC 0002-9401
- Generic Name
- Donanemab-azbt
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
Genentech, Inc.
NDC Product
Human Prescription DrugCellcept NDC 0004-0261
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCellcept NDC 0004-0298
- Generic Name
- Mycophenolate Mofetil Hydrochloride
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Diphenhydramine Hcl
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Honey Cough Dm Day Night Value Pack NDC 0031-2059
- Generic Name
- Dextromethorphan Hbr, Guaifenesin, Doxylamine Succinate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Day And Night Cough Relief Value Pack NDC 0031-2099
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Chlorpheniramine...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Childrens Honey Day Night Dm Value Pack NDC 0031-2102
- Generic Name
- Dextromethorphan Hbr, Guaifenesin, Doxylamine Succinate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Day And Night Maximum Strength Cough Dm NDC 0031-2103
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succi...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Day And Night Cough Relief Dm Max NDC 0031-2834
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succi...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Cough Long-acting NDC 0031-8694
- Generic Name
- Dextromethorphan Hydrobromide
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Cough And Chest Congestion Dm NDC 0031-8702
- Generic Name
- Dextromethorphan Hydrobromide And Guaifenesin
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Cough And Chest Congestion Dm NDC 0031-8715
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Cough And Cold Cf NDC 0031-8716
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrin...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Maximum Strength Nighttime Cough Dm NDC 0031-8718
- Generic Name
- Dextromethorphan Hydrobromide, Doxylamine Succinate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Bulk Ingredient- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hy...
- Dosage Form
- Syrup
- Route
- N/A
- Marketing
- EXPORT ONLY
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Peak Cold Multi-symptom Cold NDC 0031-8742
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrin...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Severe Multi-symptom Cough Cold Flu NDC 0031-8751
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, P...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Severe Multi-symptom Cough Cold Flu Nighttime NDC 0031-8752
- Generic Name
- Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine ...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Cough Plus Chest Congestion Dm NDC 0031-8757
- Generic Name
- Dextromethorphan Hydrobromide And Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Honey Cough And Chest Congestion Dm NDC 0031-8760
- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Honey Severe Cough, Flu Plus Sore Throat NDC 0031-8771
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime NDC 0067-0100
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime Honey Ginger NDC 0067-0103
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Chest Congestion Daytime NDC 0067-0104
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Nighttime NDC 0067-0105
- Generic Name
- Acetaminophen, Diphenhydramine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime Berry Burst NDC 0067-0106
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief NDC 0067-0107
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Diphenphydramine Hcl, G...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Pseudoephedrine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Total Relief Maximum Strength NDC 0067-0118
- Generic Name
- Calcium Carbonate, Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Total Relief Maximum Strength NDC 0067-0119
- Generic Name
- Calcium Carbonate, Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Combo Pack NDC 0067-0122
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Diphenhydramine Hcl
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Combo Pack NDC 0067-0123
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Diphenhydramine Hcl
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Powerpods Daytime Severe Cold NDC 0067-6094
- Generic Name
- Acetaminophen, Dextromethorphan, Phenylephrine
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Powerpods Nighttime Severe Cold NDC 0067-6095
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Multi-symptom Severe Cold NDC 0067-6426
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime Berry Burst NDC 0067-6800
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hydrochlo...
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Nighttime NDC 0067-6801
- Generic Name
- Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine ...
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime NDC 0067-6802
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Nighttime NDC 0067-6803
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl, Diph...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Daytime Severe Cold And Cough NDC 0067-7917
- Generic Name
- Acetaminophen, Dextromethorphan, Phenylephrine
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Nighttime Severe Cold And Cough NDC 0067-7918
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl, Diph...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Daytime NDC 0067-7921
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Nighttime NDC 0067-7922
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, And Acetaminophen, Chlo...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Daytime Nighttime Value Pack NDC 0067-8125
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl And A...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Daytime Severe Cold And Cough NDC 0067-8127
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Nighttime Severe Cold And Cough NDC 0067-8129
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Severe Cold And Flu Syrup NDC 0067-8132
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephr...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Daytime NDC 0067-8204
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Nighttime NDC 0067-8205
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, And Acetaminophen, Chlo...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugOndansetron Hydrochloride NDC 0054-0064
- Generic Name
- Ondansetron Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBuprenorphine NDC 0054-0176
- Generic Name
- Buprenorphine
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBuprenorphine NDC 0054-0177
- Generic Name
- Buprenorphine
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Buprenorphine Hydrochloride And Naloxone Hydrochloride Dihyd...
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Buprenorphine Hydrochloride And Naloxone Hydrochloride Dihyd...
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlendronate Sodium NDC 0054-0282
- Generic Name
- Alendronate Sodium
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLinezolid NDC 0054-0319
- Generic Name
- Linezolid
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRufinamide NDC 0054-0528
- Generic Name
- Rufinamide
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrocodone Bitartrate And Acetaminophen NDC 0054-0843
- Generic Name
- Hydrocodone Bitartrate And Acetaminophen
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAminocaproic Acid NDC 0054-1100
- Generic Name
- Aminocaproic Acid
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugDiazepam Intensol NDC 0054-3185
- Generic Name
- Diazepam Intensol
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiazepam NDC 0054-3188
- Generic Name
- Diazepam
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiphenoxylate Hydrochloride And Atropine Sulfate NDC 0054-3194
- Generic Name
- Diphenoxylate Hydrochloride And Atropine Sulfate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethadone Hydrochloride NDC 0054-3555
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethadone Hydrochloride NDC 0054-3556
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMidazolam Hydrochloride NDC 0054-3566
- Generic Name
- Midazolam Hydrochloride
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDocetaxel NDC 0143-9204
- Generic Name
- Docetaxel
- Dosage Form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDocetaxel NDC 0143-9205
- Generic Name
- Docetaxel
- Dosage Form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDacarbazine NDC 0143-9245
- Generic Name
- Dacarbazine
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcetaminophen NDC 0143-9386
- Generic Name
- Acetaminophen
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGranisetron Hydrochloride NDC 0143-9744
- Generic Name
- Granisetron Hydrochloride
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGranisetron Hydrochloride NDC 0143-9745
- Generic Name
- Granisetron Hydrochloride
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0143-9872
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
Hikma Pharmceuticals USA Inc.
NDC Product
Human Prescription DrugOxycodone Hydrochloride NDC 0054-0390
- Generic Name
- Oxycodone Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Severe Nighttime NDC 0113-0019
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, P...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Pain And Fever NDC 0113-0020
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen Infants NDC 0113-0057
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Pain And Fever NDC 0113-0161
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen Childrens NDC 0113-0166
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Sleep Time NDC 0113-0186
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens All Day Allergy NDC 0113-0189
- Generic Name
- Cetirizine Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Pain And Fever NDC 0113-0212
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Night Time NDC 0113-0335
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Allergy NDC 0113-0379
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nighttime NDC 0113-0459
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens All Day Allergy NDC 0113-0503
- Generic Name
- Cetirizine Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Pain And Fever NDC 0113-0608
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen Childrens NDC 0113-0660
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen NDC 0113-0685
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Severe Nighttime Cold And Flu NDC 0113-0763
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, P...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen Childrens NDC 0113-0897
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Tussin Dm Max NDC 0113-0927
- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Pain And Fever Infants NDC 0113-0946
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Cold And Cough NDC 0113-0987
- Generic Name
- Brompheniramine Maleate, Dextromethorphan Hbr, Phenylephrine...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Antidiarrheal NDC 0113-1645
- Generic Name
- Loperamide Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Tussin Dm NDC 0113-1725
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Lice Killing Creme Rinse NDC 0113-1910
- Generic Name
- Permethrin
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Tussin NDC 0113-2009
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Day Time Cold And Flu NDC 0113-2299
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, P...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Night Time Cold And Flu NDC 0113-2501
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Suc...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Night Time NDC 0113-6012
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Suc...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Cold Cough NDC 0113-6019
- Generic Name
- Brompheniramine Maleate, Dextromethorphan Hydrobromide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Pain And Fever NDC 0113-8959
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugStromectol NDC 0006-0032
- Generic Name
- Ivermectin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNoxafil NDC 0085-2224
- Generic Name
- Posaconazole
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Mission Pharmacal Company
NDC Product
Human Prescription DrugUrocit-k NDC 0178-0610
- Generic Name
- Potassium Citrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugUrocit-k NDC 0178-0615
- Generic Name
- Potassium Citrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
PAI Holdings, LLC dba PAI Pharma
NDC Product
Human Prescription DrugPotassium Citrate And Citric Acid NDC 0121-0676
- Generic Name
- Potassium Citrate And Citric Acid Monohydrate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugTricitrates NDC 0121-0677
- Generic Name
- Potassium Citrate, Sodium Citrate, And Citric Acid Monohydra...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 0121-0744
- Generic Name
- Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen Oral Suspension NDC 0121-0833
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSulfamethoxazole And Trimethoprim NDC 0121-0853
- Generic Name
- Sulfamethoxazole And Trimethoprim
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSulfatrim NDC 0121-0854
- Generic Name
- Sulfamethoxazole And Trimethoprim
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugDiphenhydramine Hcl NDC 0121-0865
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugOndansetron NDC 0121-0882
- Generic Name
- Ondansetron
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisolone NDC 0121-0885
- Generic Name
- Prednisolone
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhenytoin NDC 0121-0892
- Generic Name
- Phenytoin
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugDocusate Sodium NDC 0121-0935
- Generic Name
- Docusate Sodium
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-0941
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 0121-0948
- Generic Name
- Potassium Chloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugDye Free Childrens Ibuprofen NDC 0121-1022
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLithium NDC 0121-1027
- Generic Name
- Lithium
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydroxyzine Hydrochloride NDC 0121-1034
- Generic Name
- Hydroxyzine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrocodone Bitartrate And Homatropine Methylbromide NDC 0121-1036
- Generic Name
- Hydrocodone Bitartrate And Homatropine Methylbromide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugNystatin NDC 0121-1045
- Generic Name
- Nystatin
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-1047
- Generic Name
- Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 0121-1488
- Generic Name
- Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen Oral Suspension NDC 0121-1666
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugDiphenhydramine Hcl NDC 0121-1730
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 0121-1744
- Generic Name
- Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDocusate Sodium NDC 0121-1870
- Generic Name
- Docusate Sodium
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-1882
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 0121-1896
- Generic Name
- Potassium Chloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-2094
- Generic Name
- Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGuaifenesin NDC 0121-2232
- Generic Name
- Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-2823
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 0121-2847
- Generic Name
- Potassium Chloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-3141
- Generic Name
- Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugLithium NDC 0121-4027
- Generic Name
- Lithium
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 0121-4948
- Generic Name
- Potassium Chloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma
NDC Product
Human Prescription DrugBuprenorphine And Naloxone NDC 0121-1018
- Generic Name
- Buprenorphine Hydrochloride And Naloxone Hydrochloride
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBuprenorphine Hydrochloride NDC 0121-1019
- Generic Name
- Buprenorphine Hydrochloride
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBuprenorphine And Naloxone NDC 0121-2036
- Generic Name
- Buprenorphine Hydrochloride And Naloxone Hydrochloride
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBuprenorphine Hydrochloride NDC 0121-2038
- Generic Name
- Buprenorphine Hydrochloride
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
Person and Covey
NDC Product
Human Otc DrugSolbar Shield Spf40 NDC 0096-0682
- Generic Name
- Solbar Shield Spf40
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Zinc Spf38 NDC 0096-0688
- Generic Name
- Solbar Zinc Spf38
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDhs Tar Gel NDC 0096-0736
- Generic Name
- Coal Tar
- Dosage Form
- Shampoo
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDhs Tar NDC 0096-0737
- Generic Name
- Coal Tar
- Dosage Form
- Shampoo
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Pharmaceutical Associates, Inc.
NDC Product
Human Prescription DrugSodium Citrate And Citric Acid NDC 0121-0595
- Generic Name
- Sodium Citrate And Citric Acid Monohydrate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugDiazepam NDC 0121-0905
- Generic Name
- Diazepam
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen Oral Suspension NDC 0121-0914
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSodium Citrate And Citric Acid NDC 0121-1190
- Generic Name
- Sodium Citrate And Citric Acid Monohydrate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0093-2277
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0093-2279
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 0093-4136
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 0093-4137
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugArformoterol Tartrate NDC 0093-5955
- Generic Name
- Arformoterol Tartrate
- Dosage Form
- Solution
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0093-8675
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMesalamine NDC 0093-9224
- Generic Name
- Mesalamine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
UCB, Inc.
NDC Product
Human Prescription DrugVimpat NDC 0131-5410
- Generic Name
- Lacosamide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugTorisel NDC 0008-1179
- Generic Name
- Temsirolimus
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Xttrium Laboratories, Inc
NDC Product
Human Prescription DrugAmantadine NDC 0116-4010
- Generic Name
- Amantadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Promethazine Hydrochloride And Dextromethorphan Hydrobromide
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- ANDA
Active Listing
Xttrium Laboratories, Inc.
NDC Product
Human Prescription DrugMegestrol Acetate NDC 0116-4011
- Generic Name
- Megestrol Acetate
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPromethazine Hydrochloride NDC 0116-4023
- Generic Name
- Promethazine Hydrochloride
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNystatin Oral Suspension NDC 0116-4026
- Generic Name
- Nystatin
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
