NDC Product
Human Prescription DrugOrilissa NDC 0074-0038
- Generic Name
- Elagolix
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Starch, Corn, uniquely identified by the FDA Unique Ingredient Identifier (UNII) O8232NY3SJ.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9005-25-8 and the RxNorm Concept ID (RxCUI) 1039062. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
STARCH, CORN
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
O8232NY3SJ
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
mixture
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Starch, Corn. 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
ZEA MAYS (CORN) STARCH
OF
Common Names & Synonyms
CORN STARCH
CN
CORN STARCH (PREGELATINIZED)
CN
CORN STARCH [JAN]
CN
CORN STARCH [VANDF]
CN
CORN STARCH PREPARATION
CN
CORN STARCH, PREGELATINIZED
CN
CORNSTARCH
CN
KOI [JAN]
CN
MAIZE STARCH
CN
MAIZE STARCH [EP IMPURITY]
CN
MAIZE STARCH [EP MONOGRAPH]
CN
NTX-1 COMPONENT CORN STARCH
CN
PREGELATINIZED CORN STARCH 1551
CN
STARCH 1500
CN
STARCH 1500 PREGELATINIZED
CN
STARCH 1500, PREGELATINIZED
CN
STARCH 1500, PREGELATINIZED [II]
CN
STARCH 1551
CN
STARCH 1551 [II]
CN
STARCH MAIZE PREGELATINIZED
CN
STARCH, CORN
CN
STARCH, CORN (SPRESS B820)
CN
STARCH, CORN [II]
CN
STARCH, MAIZE
CN
STARCH, PREGELATINIZED CORN
CN
STARCH, PREGELATINIZED CORN [II]
CN
TOPICAL STARCH
CN
TOPICAL STARCH [USP MONOGRAPH]
CN
ZEA MAYS STARCH [WHO-DD]
CN
Brand / Trade Names
NATIONAL 78-1551
BN
SUPERSTARCH 200
BN
UNI-PURE FL
BN
UNI-PURE WG 220
BN
NDC Products Containing STARCH, CORN
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 DrugOrilissa NDC 0074-0039
- Generic Name
- Elagolix
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
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
Genentech, Inc.
NDC Product
Human Prescription DrugCellcept NDC 0004-0259
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
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
NDC Product
Human Prescription DrugTamiflu NDC 0004-0800
- Generic Name
- Oseltamivir Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTamiflu NDC 0004-0802
- Generic Name
- Oseltamivir Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTamiflu NDC 0004-0822
- Generic Name
- Oseltamivir Phosphate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugRobitussin Direct Sore Throat Pain NDC 0031-9301
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Coated
- 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 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 DrugExcedrin Extra Strength Headache NDC 0067-2003
- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Pm Triple Action Caplets NDC 0067-2056
- Generic Name
- Acetaminophen, Aspirin (nsaid) And Diphenhydramine Citrate
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Rapid Relief NDC 0067-2200
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Daytime Severe Cold And Cough NDC 0067-8136
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Nighttime Severe Cold And Cough NDC 0067-8137
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Tension Headache NDC 0067-8139
- Generic Name
- Acetaminophen, Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEx-lax Regular Strength Stimulant Laxative NDC 0067-8141
- Generic Name
- Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEx-lax Maximum Strength Stimulant Laxative NDC 0067-8142
- Generic Name
- Sennosides
- Dosage Form
- Pill
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPerdiem NDC 0067-8143
- Generic Name
- Sennosides, Stimulant Laxative
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Severe Cold And Flu Caplets NDC 0067-8145
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephr...
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine, And Diphenhydramin...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine, And Diphenhydramin...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength And Excedrin Tension Headache NDC 0067-8151
- Generic Name
- Acetaminophen, Aspirin (nsaid), And Caffeine
- Dosage Form
- Kit
- Route
- N/A
- 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 DrugExcedrin Extra Strength Pain Reliever NDC 0067-8202
- Generic Name
- Acetaminophen, Aspirin (nsaid), And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength Pain Reliever NDC 0067-8203
- Generic Name
- Acetaminophen, Aspirin (nsaid), And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
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
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugFlecainide Acetate NDC 0054-0010
- Generic Name
- Flecainide Acetate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFlecainide Acetate NDC 0054-0011
- Generic Name
- Flecainide Acetate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFlecainide Acetate NDC 0054-0012
- Generic Name
- Flecainide Acetate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-0017
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-0018
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-0019
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZaleplon NDC 0054-0084
- Generic Name
- Zaleplon
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZaleplon NDC 0054-0085
- Generic Name
- Zaleplon
- 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 DrugAcarbose NDC 0054-0140
- Generic Name
- Acarbose
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcarbose NDC 0054-0141
- Generic Name
- Acarbose
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcarbose NDC 0054-0142
- Generic Name
- Acarbose
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0054-0163
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0054-0166
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Tablet
- 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 DrugMorphine Sulfate NDC 0054-0235
- Generic Name
- Morphine Sulfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0054-0236
- Generic Name
- Morphine Sulfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCodeine Sulfate NDC 0054-0243
- Generic Name
- Codeine Sulfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCodeine Sulfate NDC 0054-0244
- Generic Name
- Codeine Sulfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCodeine Sulfate NDC 0054-0245
- Generic Name
- Codeine Sulfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0054-0283
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0054-0284
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet
- 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 DrugRufinamide NDC 0054-0425
- Generic Name
- Rufinamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRufinamide NDC 0054-0426
- Generic Name
- Rufinamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevorphanol Tartrate NDC 0054-0438
- Generic Name
- Levorphanol Tartrate
- Dosage Form
- Tablet
- 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 DrugMethadone Hydrochloride NDC 0054-0709
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethadone Hydrochloride NDC 0054-0710
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Tablet
- 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 DrugEltrombopag NDC 0054-0962
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 0054-0963
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 0054-0964
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 0054-0965
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet
- 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 DrugFurosemide NDC 0054-3294
- Generic Name
- Furosemide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-3298
- Generic Name
- Furosemide
- 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 DrugPrednisone Intensol NDC 0054-3721
- Generic Name
- Prednisone Intensol
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-3722
- Generic Name
- Prednisone
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-4297
- Generic Name
- Furosemide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-4299
- Generic Name
- Furosemide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-4301
- Generic Name
- Furosemide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLeucovorin Calcium NDC 0054-4496
- Generic Name
- Leucovorin Calcium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLeucovorin Calcium NDC 0054-4497
- Generic Name
- Leucovorin Calcium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLeucovorin Calcium NDC 0054-4498
- Generic Name
- Leucovorin Calcium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLeucovorin Calcium NDC 0054-4499
- Generic Name
- Leucovorin Calcium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiskets NDC 0054-4538
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMethotrexate Sodium NDC 0054-4550
- Generic Name
- Methotrexate Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMercaptopurine NDC 0054-4581
- Generic Name
- Mercaptopurine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-4728
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-4741
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-4742
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-8297
- Generic Name
- Furosemide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-8299
- Generic Name
- Furosemide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFurosemide NDC 0054-8301
- Generic Name
- Furosemide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLeucovorin Calcium NDC 0054-8496
- Generic Name
- Leucovorin Calcium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-8724
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-8739
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-8740
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-9817
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-9818
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-9828
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
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 0054-4179
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4180
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4181
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- 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
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugStromectol NDC 0006-0032
- Generic Name
- Ivermectin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugFemara NDC 0078-0249
- Generic Name
- Letrozole
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMyfortic NDC 0078-0385
- Generic Name
- Mycophenolic Acid
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMyfortic NDC 0078-0386
- Generic Name
- Mycophenolic Acid
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEgaten NDC 0078-0937
- Generic Name
- Triclabendazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Parke-Davis Div of Pfizer Inc
NDC Product
Human Prescription DrugCelontin NDC 0071-0525
- Generic Name
- Methsuximide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugLomotil NDC 0025-0061
- Generic Name
- Diphenoxylate Hydrochloride And Atropine Sulfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAldactone NDC 0025-1001
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAldactone NDC 0025-1031
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAldactone NDC 0025-1041
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugArthrotec NDC 0025-1411
- Generic Name
- Diclofenac Sodium And Misoprostol
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugArthrotec NDC 0025-1421
- Generic Name
- Diclofenac Sodium And Misoprostol
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFlagyl NDC 0025-1942
- Generic Name
- Metronidazole
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNorpace Cr NDC 0025-2732
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNorpace Cr NDC 0025-2742
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNorpace NDC 0025-2752
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNorpace NDC 0025-2762
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTikosyn NDC 0069-5800
- Generic Name
- Dofetilide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTikosyn NDC 0069-5810
- Generic Name
- Dofetilide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTikosyn NDC 0069-5820
- Generic Name
- Dofetilide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Pharmacia & Upjohn Company LLC
NDC Product
Human Prescription DrugCortef NDC 0009-0012
- Generic Name
- Hydrocortisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugHalcion NDC 0009-0017
- Generic Name
- Triazolam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0020
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0022
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCortef NDC 0009-0031
- Generic Name
- Hydrocortisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCortef NDC 0009-0044
- Generic Name
- Hydrocortisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0056
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0073
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCleocin Hydrochloride NDC 0009-0225
- Generic Name
- Clindamycin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCleocin Hydrochloride NDC 0009-0331
- Generic Name
- Clindamycin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCleocin Hydrochloride NDC 0009-0395
- Generic Name
- Clindamycin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
ROERIG
NDC Product
Human Prescription DrugGeodon NDC 0049-0056
- Generic Name
- Ziprasidone Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGeodon NDC 0049-0058
- Generic Name
- Ziprasidone Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGeodon NDC 0049-0352
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGeodon NDC 0049-0354
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGeodon NDC 0049-0356
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Sanofi-Aventis U.S. LLC
NDC Product
Human Prescription DrugPrimaquine Phosphate NDC 0024-1596
- Generic Name
- Primaquine Phosphate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMultaq NDC 0024-4142
- Generic Name
- Dronedarone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 0093-0010
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMoexipril Hydrochloride NDC 0093-0017
- Generic Name
- Moexipril Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 0093-0018
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLoperamide Hydrochloride NDC 0093-0311
- Generic Name
- Loperamide Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLovastatin NDC 0093-0576
- Generic Name
- Lovastatin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPiroxicam NDC 0093-0756
- Generic Name
- Piroxicam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPiroxicam NDC 0093-0757
- Generic Name
- Piroxicam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
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 DrugLovastatin NDC 0093-0926
- Generic Name
- Lovastatin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLovastatin NDC 0093-0928
- Generic Name
- Lovastatin
- Dosage Form
- Tablet
- 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 DrugNystatin NDC 0093-0983
- Generic Name
- Nystatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Nystatin
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugSotalol Hydrochloride NDC 0093-1060
- Generic Name
- Sotalol Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSotalol Hydrochloride NDC 0093-1061
- Generic Name
- Sotalol Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSotalol Hydrochloride NDC 0093-1062
- Generic Name
- Sotalol Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSotalol Hydrochloride NDC 0093-1063
- Generic Name
- Sotalol Hydrochloride
- 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 DrugCilostazol NDC 0093-2064
- Generic Name
- Cilostazol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCilostazol NDC 0093-2065
- Generic Name
- Cilostazol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDoxazosin NDC 0093-2067
- Generic Name
- Doxazosin Mesylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDoxazosin NDC 0093-2068
- Generic Name
- Doxazosin Mesylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDoxazosin NDC 0093-2069
- Generic Name
- Doxazosin Mesylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDoxazosin NDC 0093-2070
- Generic Name
- Doxazosin Mesylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLiothyronine Sodium NDC 0093-2178
- Generic Name
- Liothyronine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLiothyronine Sodium NDC 0093-2179
- Generic Name
- Liothyronine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLiothyronine Sodium NDC 0093-2180
- Generic Name
- Liothyronine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoclopramide NDC 0093-2203
- Generic Name
- Metoclopramide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoclopramide NDC 0093-2204
- Generic Name
- Metoclopramide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSucralfate NDC 0093-2210
- Generic Name
- Sucralfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Quinine Sulfate
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugQuinine Sulfate NDC 0093-3002
- Generic Name
- Quinine Sulfate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0093-3008
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0093-3009
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Viatris Specialty LLC
NDC Product
Human Prescription DrugUrelle NDC 0037-6321
- Generic Name
- Hyoscyamine Sulfate, Methenamine, Methylene Blue, Phenyl Sal...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
sanofi-aventis U.S. LLC
NDC Product
Human Prescription DrugPriftin NDC 0088-2102
- Generic Name
- Rifapentine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
