NDC Product
Human Prescription DrugKaletra NDC 0074-3956
- Generic Name
- Lopinavir And Ritonavir
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Glycerin, uniquely identified by the FDA Unique Ingredient Identifier (UNII) PDC6A3C0OX.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 56-81-5 and the RxNorm Concept ID (RxCUI) 4910. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
GLYCERIN
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
PDC6A3C0OX
The specific atomic composition represented as a molecular structure string.
InChIKey
C3H8O3 International Chemical Identifier digital signature for unique molecular identification.
SMILES String
PEDCQBHIVMGVHV-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.
INN ID
444
Sequential identifier assigned via the WHO International Nonproprietary Name program.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
C(C(CO)O)O
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Glycerin. 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
GLYCERIN
OF
GLYCEROL
OF
Common Names & Synonyms
GLYCERIN [HSDB]
CN
GLYCERIN [II]
CN
GLYCERIN [JAN]
CN
GLYCERIN [ORANGE BOOK]
CN
GLYCERIN [USP MONOGRAPH]
CN
GLYCERIN [USP-RS]
CN
GLYCERIN [VANDF]
CN
GLYCERIN,ANHYDROUS
CN
GLYCERIN,ANHYDROUS [VANDF]
CN
GLYCERINUM
CN
GLYCERINUM [HPUS]
CN
GLYCEROL [EP IMPURITY]
CN
GLYCEROL [EP MONOGRAPH]
CN
GLYCEROL [FHFI]
CN
GLYCEROL [INN]
CN
GLYCEROL [MART.]
CN
GLYCEROL [MI]
CN
GLYCEROL [WHO-DD]
CN
GLYCEROL [WHO-IP]
CN
GLYCEROL 85% [WHO-DD]
CN
GLYCEROLUM [WHO-IP LATIN]
CN
MONOCTANOIN COMPONENT D
CN
TRYHYDROXYPROPANE
CN
Systematic Nomenclature
1,2,3-PROPANETRIOL
SYS
1,2,3-TRIHYDROXYPROPANE
SYS
2-PROPANOL, 1,3-DIHYDROXY-
SYS
GLYCERINE
SYS
Technical Codes
E-422
CD
FEMA NO. 2525
CD
INS NO.422
CD
INS-422
CD
M 314429
CD
NSC-9230
CD
PZN 7474853
CD
NDC Products Containing GLYCERIN
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 DrugKaletra NDC 0074-6799
- Generic Name
- Lopinavir And Ritonavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZemplar NDC 0074-9036
- Generic Name
- Paricalcitol
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZemplar NDC 0074-9037
- Generic Name
- Paricalcitol
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
Alcon Laboratories, Inc.
NDC Product
Human Prescription DrugBetadine NDC 0065-0411
- Generic Name
- Povidone-iodine
- Dosage Form
- Solution
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugGenteal Tears (moderate) NDC 0065-0426
- Generic Name
- Dextran 70, Glycerin, Hypromellose
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugZaditor NDC 0065-4011
- Generic Name
- Ketotifen Fumarate
- Dosage Form
- Solution
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugInveltys NDC 0065-9307
- Generic Name
- Loteprednol Etabonate
- Dosage Form
- Suspension
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
Allergan, Inc.
NDC Product
Human Otc DrugSkinmedica Acne Clarifying Treatment NDC 0023-1230
- Generic Name
- Salicylic Acid
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRefresh Tears Pf NDC 0023-3110
- Generic Name
- Carboxymethylcellulose Sodium, Glycerin
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRefresh Optive NDC 0023-3240
- Generic Name
- Carboxymethylcellulose Sodium And Glycerin
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRefresh Optive NDC 0023-3416
- Generic Name
- Carboxymethylcellulose Sodium, Glycerin
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRefresh Relieva Pf Xtra NDC 0023-3782
- Generic Name
- Carboxymethylcellulose Sodium And Glycerin
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRefresh Optive Mega-3 Pf NDC 0023-3988
- Generic Name
- Carboxymethylcellulose Sodium, Glycerin, Polysorbate 80
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRefresh Optive Advanced NDC 0023-4307
- Generic Name
- Carboxymethylcellulose Sodium, Glycerin, And Polysorbate 80
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRefresh Optive Advanced NDC 0023-4491
- Generic Name
- Carboxymethylcellulose Sodium, Glycerin, Polysorbate 80
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRefresh Relieva Pf NDC 0023-4515
- Generic Name
- Carboxymethylcellulose Sodium And Glycerin
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugRestasis Multidose NDC 0023-5301
- Generic Name
- Cyclosporine
- Dosage Form
- Emulsion
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugRefresh Optive Drops NDC 0023-5459
- Generic Name
- Carboxymethylcellulose Sodium And Glycerin
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTotal Defense Repair Broad Spectrum Spf 34 Sunscreen NDC 0023-5494
- Generic Name
- Octinoxate, Octisalate And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Octinoxate, Octisalate, Titanium Dioxide And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Zinc Oxide And Octinoxate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRefresh Optive Mega-3 NDC 0023-5773
- Generic Name
- Carboxymethylcellulose Sodium, Glycerin And Polysorbate 80
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
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
NDC Product
Human Prescription DrugCrinone NDC 0023-6150
- Generic Name
- Progesterone
- Dosage Form
- Gel
- Route
- Vaginal
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCrinone NDC 0023-6151
- Generic Name
- Progesterone
- Dosage Form
- Gel
- Route
- Vaginal
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugRefresh Relieva NDC 0023-6630
- Generic Name
- Carboxymethylcellulose Sodium, Glycerin
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRefresh Relieva Preservative Free NDC 0023-6634
- Generic Name
- Carboxymethylcellulose Sodium And Glycerin
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRefresh Digital NDC 0023-6952
- Generic Name
- Carboxymethylcellulose Sodium, Glycerin, Polysorbate 80
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRefresh Digital Pf NDC 0023-6954
- Generic Name
- Carboxymethylcellulose Sodium, Glycerin And Polysorbate 80
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugRestasis NDC 0023-9163
- Generic Name
- Cyclosporine
- Dosage Form
- Emulsion
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
Eli Lilly and Company
NDC Product
Human Prescription DrugHumalog NDC 0002-7510
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumalog Mix75/25 NDC 0002-7511
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Suspension
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumalog NDC 0002-7516
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumalog Kwikpen NDC 0002-7712
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumalog Junior Kwikpen NDC 0002-7714
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugBasaglar Kwikpen NDC 0002-7715
- Generic Name
- Insulin Glargine
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugLyumjev NDC 0002-7726
- Generic Name
- Insulin Lispro-aabc
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugLyumjev NDC 0002-7728
- Generic Name
- Insulin Lispro-aabc
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugInsulin Lispro NDC 0002-7737
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugInsulin Lispro Junior Kwikpen NDC 0002-7752
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumatrope NDC 0002-8147
- Generic Name
- Somatropin
- Dosage Form
- Kit
- Route
- Intramuscular; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumatrope NDC 0002-8148
- Generic Name
- Somatropin
- Dosage Form
- Kit
- Route
- Intramuscular; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumatrope NDC 0002-8149
- Generic Name
- Somatropin
- Dosage Form
- Kit
- Route
- Intramuscular; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugLyumjev Kwikpen NDC 0002-8207
- Generic Name
- Insulin Lispro-aabc
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Otc DrugHumulin R NDC 0002-8215
- Generic Name
- Insulin Human
- Dosage Form
- Injection, Solution
- Route
- Parenteral
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugInsulin Lispro Kwikpen NDC 0002-8222
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugLyumjev Kwikpen NDC 0002-8228
- Generic Name
- Insulin Lispro-aabc
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Suspension
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Otc DrugHumulin N NDC 0002-8315
- Generic Name
- Insulin Human
- Dosage Form
- Injection, Suspension
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugLyumjev Junior Kwikpen NDC 0002-8351
- Generic Name
- Insulin Lispro-aabc
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumulin R U-500 NDC 0002-8501
- Generic Name
- Insulin Human
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Otc DrugHumulin 70/30 NDC 0002-8715
- Generic Name
- Insulin Human
- Dosage Form
- Injection, Suspension
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumalog Mix75/25 Kwikpen NDC 0002-8797
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Suspension
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumalog Mix50/50 Kwikpen NDC 0002-8798
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Suspension
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumalog Kwikpen NDC 0002-8799
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Otc DrugHumulin 70/30 Kwikpen NDC 0002-8803
- Generic Name
- Insulin Human
- Dosage Form
- Injection, Suspension
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Otc DrugHumulin N NDC 0002-8805
- Generic Name
- Insulin Human
- Dosage Form
- Injection, Suspension
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumulin R U-500 Kwikpen NDC 0002-8824
- Generic Name
- Insulin Human
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugRezvoglar Kwikpen NDC 0002-8980
- Generic Name
- Insulin Glargine-aglr
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
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 DrugRobitussin 12 Hour Cough Relief NDC 0031-8655
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
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
Human Otc DrugChildrens Robitussin 12 Hour Cough Relief NDC 0031-8725
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin 12 Hour Cough Relief NDC 0031-8726
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
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, And Doxylamine...
- 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 12 Hour Cough Relief NDC 0031-8753
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRobitussin 12 Hour Cough Relief NDC 0031-8754
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRobitussin 12 Hour Cough Relief NDC 0031-8755
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
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 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 Medi-soothers NDC 0031-9306
- Generic Name
- Dextromethorphan Hydrobromide, Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Medi-soothers NDC 0031-9307
- Generic Name
- Dextromethorphan Hydrobromide, Menthol
- Dosage Form
- Lozenge
- 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 DrugRobitussin Nighttime Cough Dm Soft Chews NDC 0031-9311
- Generic Name
- Dextromethorphan Hydrobromide, Doxylamine Succinate
- Dosage Form
- Tablet, Chewable
- 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 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 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 DrugGas-x Ultra Strength Antigas Softgels NDC 0067-6274
- Generic Name
- Simethicone
- Dosage Form
- Capsule, Liquid Filled
- 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 DrugGas-x Maximum Strength Softgels NDC 0067-6283
- Generic Name
- Simethicone
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Ultimate Strength Softgels NDC 0067-8075
- Generic Name
- Simethicone
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- 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
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 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 DrugCalcitriol NDC 0054-0007
- Generic Name
- Calcitriol
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDigoxin NDC 0054-0057
- Generic Name
- Digoxin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
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 DrugCevimeline Hydrochloride NDC 0054-0334
- Generic Name
- Cevimeline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPosaconazole NDC 0054-0449
- Generic Name
- Posaconazole
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIcosapent Ethyl NDC 0054-0508
- Generic Name
- Icosapent Ethyl
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0054-0517
- Generic Name
- Morphine Sulfate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
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 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 DrugIndomethacin NDC 0054-1950
- Generic Name
- Indomethacin
- Dosage Form
- Suppository
- Route
- Rectal
- 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 DrugMeperidine Hydrochloride NDC 0054-3545
- Generic Name
- Meperidine Hydrochloride
- 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
Hikma Pharmaceuticals USA, Inc.
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 0054-8174
- 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
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugTice Bcg NDC 0052-0602
- Generic Name
- Bacillus Calmette-guerin
- Dosage Form
- Powder, For Suspension
- Route
- Intravesical
- Marketing
- BLA
Active Listing
NDC Product
VaccineBcg Vaccine NDC 0052-0603
- Generic Name
- Bacillus Calmette-guerin Substrain Tice Live Antigen
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Percutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugNoxafil NDC 0085-1328
- Generic Name
- Posaconazole
- Dosage Form
- Suspension
- 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
NDC Product
Human Prescription DrugNoxafil NDC 0085-4324
- Generic Name
- Posaconazole
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNoxafil NDC 0085-4331
- Generic Name
- Posaconazole
- Dosage Form
- Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugSandimmune NDC 0078-0109
- Generic Name
- Cyclosporine
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSandimmune NDC 0078-0240
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSandimmune NDC 0078-0241
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNeoral NDC 0078-0246
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNeoral NDC 0078-0248
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNeoral NDC 0078-0274
- Generic Name
- Cyclosporine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
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
NDC Product
Human Prescription DrugRydapt NDC 0078-0698
- Generic Name
- Rydapt
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
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 Avo Spf35 NDC 0096-0687
- Generic Name
- Solbar Avo Spf35
- 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 DrugSolbar Sunscreen 35 Avo NDC 0096-0690
- Generic Name
- Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Sunscreen 40 Zinc NDC 0096-0691
- Generic Name
- Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Sunscreen 40 Shield NDC 0096-0692
- Generic Name
- Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugIdamycin Pfs NDC 0013-2576
- Generic Name
- Idarubicin Hydrochloride
- Dosage Form
- Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIdamycin Pfs NDC 0013-2586
- Generic Name
- Idarubicin Hydrochloride
- Dosage Form
- Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIdamycin Pfs NDC 0013-2596
- Generic Name
- Idarubicin Hydrochloride
- Dosage Form
- Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPropofol NDC 0069-0209
- Generic Name
- Propofol
- Dosage Form
- Injection, Emulsion
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropofol NDC 0069-0234
- Generic Name
- Propofol
- Dosage Form
- Injection, Emulsion
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropofol NDC 0069-0248
- Generic Name
- Propofol
- Dosage Form
- Injection, Emulsion
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTalzenna NDC 0069-0252
- Generic Name
- Talazoparib
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTalzenna NDC 0069-0353
- Generic Name
- Talazoparib
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTalzenna NDC 0069-0454
- Generic Name
- Talazoparib
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTalzenna NDC 0069-0546
- Generic Name
- Talazoparib
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTalzenna NDC 0069-0655
- Generic Name
- Talazoparib
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTalzenna NDC 0069-0757
- Generic Name
- Talazoparib
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVyndamax NDC 0069-8730
- Generic Name
- Tafamidis
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
Pharmacia & Upjohn Company LLC
NDC Product
Human Prescription DrugCleocin T NDC 0009-3329
- Generic Name
- Clindamycin Phosphate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- NDA
Active Listing
Sanofi-Aventis U.S. LLC
NDC Product
Human Prescription DrugSoliqua 100/33 NDC 0024-5761
- Generic Name
- Insulin Glargine And Lixisenatide
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugToujeo NDC 0024-5869
- Generic Name
- Insulin Glargine
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugToujeo Max NDC 0024-5871
- Generic Name
- Insulin Glargine
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugAdmelog NDC 0024-5924
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugAdmelog NDC 0024-5925
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugAdmelog NDC 0024-5926
- Generic Name
- Insulin Lispro
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- BLA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugImiquimod NDC 0093-3133
- Generic Name
- Imiquimod
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugCyclosporine Modified NDC 0093-9018
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclosporine Modified NDC 0093-9019
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclosporine Modified NDC 0093-9020
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
Viatris Specialty LLC
NDC Product
Human Prescription DrugDymista NDC 0037-0245
- Generic Name
- Azelastine Hydrochloride And Fluticasone Propionate
- Dosage Form
- Spray, Metered
- Route
- Nasal
- Marketing
- NDA
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugPremarin Vaginal NDC 0046-0872
- Generic Name
- Conjugated Estrogens
- Dosage Form
- Cream
- Route
- Vaginal
- Marketing
- NDA
Active Listing
sanofi-aventis U.S. LLC
NDC Product
Human Prescription DrugLantus Solostar NDC 0088-2219
- Generic Name
- Insulin Glargine
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugLantus NDC 0088-2220
- Generic Name
- Insulin Glargine
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
