NDC Product
Human Prescription DrugOriahnn NDC 0074-1017
- Generic Name
- Elagolix And Estradiol And Norethisterone
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Fd&c Red No. 40, uniquely identified by the FDA Unique Ingredient Identifier (UNII) WZB9127XOA.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 25956-17-6 and the RxNorm Concept ID (RxCUI) N/A. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
FDA UNII Code
WZB9127XOA
CAS Registry Number
25956-17-6
RxNorm Concept ID
N/A
Detailed Substance Profile
Preferred Name
FD&C RED NO. 40
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
WZB9127XOA
The specific atomic composition represented as a molecular structure string.
InChIKey
C18H14N2O8S2.2Na International Chemical Identifier digital signature for unique molecular identification.
SMILES String
CEZCCHQBSQPRMU-LLIZZRELSA-L 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
c1c(ccc2c(c(ccc21)O)/N=N/c3c(cc(c(c3)C)S(=O)(=O)[O-])OC)S(=O)([O-])=O.[Na+].[Na+]
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Fd&c Red No. 40. 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.
FDA Official Name
CI 16035
OF
CURRY RED
OF
FD&C RED NO. 40
OF
RED 40
OF
Common Names & Synonyms
2-NAPHTHALENESULFONIC ACID, 6-HYDROXY-5-((2-METHOXY-5-METHYL-4-SULFOPHENYL)AZO)-, DISODIUM SALT
CN
ALLURA RED
CN
ALLURA RED [FCC]
CN
ALLURA RED AC [MART.]
CN
ALLURA RED AC [MI]
CN
ALLURA RED AC DYE [HSDB]
CN
ALLURA RED C.I.16035
CN
CI-FOOD RED 17
CN
D&C RED NO. 40
CN
D&C RED NO. 40 [II]
CN
E129
CN
F D & C RED #40 [VANDF]
CN
F D & C RED #40 LAKE [VANDF]
CN
F D & C RED NO. 40
CN
FANCY RED
CN
FD&C RED 40
CN
FD&C RED NO. 40 [FCC]
CN
FD&C RED NO. 40 [II]
CN
FD&C RED NO.40
CN
FDC RED 40 DYE
CN
FDC RED NO. 40
CN
JAPAN FOOD RED NO. 40
CN
JAPAN RED 40
CN
Systematic Nomenclature
2-NAPHTHALENESULFONIC ACID, 6-HYDROXY-5-(2-(2-METHOXY-5-METHYL-4-SULFOPHENYL)DIAZENYL)-, SODIUM SALT (1:2)
SYS
DISODIUM 6-HYDROXY-5-((2-METHOXY-5-METHYL-4-SULFONATOPHENYL)DIAZENYL)NAPHTHALENE-2-SULFONATE
SYS
Technical Codes
CI-(1975)NO.16035
CD
E-129
CD
INS NO.129
CD
INS-129
CD
NDC Products Containing FD&C RED NO. 40
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
NDC Product
Human Prescription DrugSynthroid NDC 0074-3727
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-5182
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-6594
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-6624
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7068
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7069
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7070
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7148
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-9296
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Allergan, Inc.
NDC Product
Human Prescription DrugTaytulla NDC 0023-5862
- Generic Name
- Norethindrone Acetate And Ethinyl Estradiol, And Ferrous Fum...
- Dosage Form
- Kit
- Route
- N/A
- 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 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 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
Human Otc Drug- Generic Name
- Dextromethorphan Hydrobromide And Guaifenesin
- Dosage Form
- Capsule, Liquid Filled
- 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 DrugRobitussin Long-acting Coughgels NDC 0031-8743
- Generic Name
- Dextromethorphan Hydrobromide
- Dosage Form
- Capsule, Liquid Filled
- 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 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 DrugRobitussin Direct Cough NDC 0031-9302
- Generic Name
- Dextromethorphan Hydrobromide
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Long-acting Cough Soft Chews NDC 0031-9310
- Generic Name
- Dextromethorphan Hydrobromide
- Dosage Form
- Tablet, Chewable
- 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 DrugTheraflu Severe Cold Relief Soft Chews NDC 0067-0111
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Nighttime Soft Chews NDC 0067-0112
- Generic Name
- Acetaminophen, Diphenhydramine Hcl
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- 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 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 DrugExcedrin Extra Strength Geltabs NDC 0067-2021
- Generic Name
- Acetaminophen, Asprin, Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine Geltabs NDC 0067-2035
- Generic Name
- Acetaminophen, Asprin, Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
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 DrugGas-x Extra Strength Softgels NDC 0067-6275
- Generic Name
- Simethicone
- Dosage Form
- Capsule, Liquid Filled
- 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 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 Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr And Acetaminophen, Chlor...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hikma Pharmaceuticals USA
NDC Product
Human Prescription DrugMethadone Hydrochloride NDC 0054-0391
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethadone Hydrochloride NDC 0054-0392
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0273
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0274
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0275
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0276
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrucalopride NDC 0054-0750
- Generic Name
- Prucalopride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugProgesterone NDC 0054-0829
- Generic Name
- Progesterone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugProgesterone NDC 0054-0830
- Generic Name
- Progesterone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugBalsalazide Disodium NDC 0054-0079
- Generic Name
- Balsalazide Disodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCalcium Acetate NDC 0054-0088
- Generic Name
- Calcium Acetate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRamipril NDC 0054-0106
- Generic Name
- Ramipril
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRamipril NDC 0054-0107
- Generic Name
- Ramipril
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRamipril NDC 0054-0108
- Generic Name
- Ramipril
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRamipril NDC 0054-0109
- Generic Name
- Ramipril
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGalantamine Hydrobromide NDC 0054-0137
- Generic Name
- Galantamine Hydrobromide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclophosphamide NDC 0054-0382
- Generic Name
- Cyclophosphamide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCyclophosphamide NDC 0054-0383
- Generic Name
- Cyclophosphamide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugHydromorphone Hydrochloride NDC 0054-0386
- Generic Name
- Hydromorphone Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDesvenlafaxine NDC 0054-0400
- Generic Name
- Desvenlafaxine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDesvenlafaxine NDC 0054-0401
- Generic Name
- Desvenlafaxine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDesvenlafaxine NDC 0054-0603
- Generic Name
- Desvenlafaxine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 0054-0622
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Butalbital, Acetaminophen, Caffeine And Codeine Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 0054-0748
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Capsule
- 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 DrugLithium Carbonate NDC 0054-2526
- Generic Name
- Lithium Carbonate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLithium Carbonate NDC 0054-2527
- Generic Name
- Lithium Carbonate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLithium Carbonate NDC 0054-2531
- Generic Name
- Lithium Carbonate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Butalbital, Acetaminophen, Caffeine And Codeine Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
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 DrugLithium Carbonate NDC 0054-8526
- Generic Name
- Lithium Carbonate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLithium Carbonate NDC 0054-8527
- Generic Name
- Lithium Carbonate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Hikma Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugDexamethasone Intensol NDC 0054-3176
- Generic Name
- Dexamethasone Intensol
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-3177
- Generic Name
- Dexamethasone
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4182
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4183
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4184
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4186
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8174
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8175
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8176
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8179
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8180
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8181
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8183
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- 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
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugTegretol NDC 0078-0509
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol Xr NDC 0078-0510
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol Xr NDC 0078-0511
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol Xr NDC 0078-0512
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Parke-Davis Div of Pfizer Inc
NDC Product
Human Prescription DrugZarontin NDC 0071-2418
- Generic Name
- Ethosuximide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugZithromax NDC 0069-3120
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZithromax NDC 0069-3130
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZithromax NDC 0069-3140
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZithromax NDC 0069-4061
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Roerig
NDC Product
Human Prescription DrugDiflucan NDC 0049-3450
- Generic Name
- Fluconazole
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0093-0810
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0093-0811
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0093-0812
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0093-0813
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiclofenac Potassium NDC 0093-0948
- Generic Name
- Diclofenac Potassium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefprozil NDC 0093-1077
- Generic Name
- Cefprozil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefprozil NDC 0093-1078
- Generic Name
- Cefprozil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEtodolac NDC 0093-1118
- Generic Name
- Etodolac
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEtodolac NDC 0093-1122
- Generic Name
- Etodolac
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcitretin NDC 0093-1135
- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugAcitretin NDC 0093-1136
- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugAcitretin NDC 0093-1138
- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1712
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1713
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1714
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1715
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1716
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1718
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1720
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1721
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 0093-1920
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 0093-1921
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAzithromycin NDC 0093-2026
- Generic Name
- Azithromycin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAzithromycin NDC 0093-2027
- Generic Name
- Azithromycin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-2267
- Generic Name
- Amoxicillin
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-2268
- Generic Name
- Amoxicillin
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-3107
- Generic Name
- Amoxicillin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-3109
- Generic Name
- Amoxicillin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicloxacillin Sodium NDC 0093-3123
- Generic Name
- Dicloxacillin Sodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicloxacillin Sodium NDC 0093-3125
- Generic Name
- Dicloxacillin Sodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDisopyramide Phosphate NDC 0093-3127
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDisopyramide Phosphate NDC 0093-3129
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-3145
- Generic Name
- Cephalexin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-3147
- Generic Name
- Cephalexin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 0093-3160
- Generic Name
- Cefdinir
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefadroxil NDC 0093-3196
- Generic Name
- Cefadroxil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugReclipsen 28 Day NDC 0093-3304
- Generic Name
- Desogestrel And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrazosin Hydrochloride NDC 0093-4068
- Generic Name
- Prazosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrazosin Hydrochloride NDC 0093-4069
- Generic Name
- Prazosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPenicillin V Potassium NDC 0093-4125
- Generic Name
- Penicillin V Potassium
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPenicillin V Potassium NDC 0093-4127
- Generic Name
- Penicillin V Potassium
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-4155
- Generic Name
- Amoxicillin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-4175
- Generic Name
- Cephalexin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-4177
- Generic Name
- Cephalexin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide NDC 0093-5002
- Generic Name
- Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide NDC 0093-5003
- Generic Name
- Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide NDC 0093-5004
- Generic Name
- Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide NDC 0093-5005
- Generic Name
- Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide NDC 0093-5006
- Generic Name
- Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5045
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5046
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 0093-5346
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 0093-5347
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 0093-5348
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5503
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5504
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5505
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5506
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5507
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugPremarin NDC 0046-1100
- Generic Name
- Estrogens, Conjugated
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPremarin NDC 0046-1102
- Generic Name
- Estrogens, Conjugated
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPremarin NDC 0046-1103
- Generic Name
- Estrogens, Conjugated
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPremarin NDC 0046-1104
- Generic Name
- Estrogens, Conjugated
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrempro NDC 0046-1105
- Generic Name
- Conjugated Estrogens And Medroxyprogesterone Acetate
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrempro NDC 0046-1106
- Generic Name
- Conjugated Estrogens And Medroxyprogesterone Acetate
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrempro NDC 0046-1107
- Generic Name
- Conjugated Estrogens And Medroxyprogesterone Acetate
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrempro NDC 0046-1108
- Generic Name
- Conjugated Estrogens And Medroxyprogesterone Acetate
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPremphase NDC 0046-2575
- Generic Name
- Conjugated Estrogens And Medroxyprogesterone Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
