NDC Product
Human Prescription DrugCreon NDC 0032-1203
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- BLA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Gelatin, Unspecified, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 2G86QN327L.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9000-70-8 and the RxNorm Concept ID (RxCUI) 4716. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
GELATIN, UNSPECIFIED
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
2G86QN327L
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 Gelatin, Unspecified. 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
GELATIN
OF
Common Names & Synonyms
GELATIN [EP MONOGRAPH]
CN
GELATIN [FCC]
CN
GELATIN [GREEN BOOK]
CN
GELATIN [HSDB]
CN
GELATIN [II]
CN
GELATIN [JAN]
CN
GELATIN [MART.]
CN
GELATIN [MI]
CN
GELATIN [USP-RS]
CN
GELATIN [VANDF]
CN
GELATIN [WHO-DD]
CN
GELATIN [WHO-IP]
CN
GELATIN LIMED BONE
CN
GELATIN, UNSPECIFIED
CN
GELATIN, UNSPECIFIED [GREEN BOOK]
CN
GELATIN,ABSORBABLE
CN
GELATIN,ABSORBABLE [VANDF]
CN
GELATIN,ABSORBABLE FILM
CN
GELATIN,ABSORBABLE FILM [VANDF]
CN
GELATIN,ABSORBABLE POWDER
CN
GELATIN,ABSORBABLE POWDER [VANDF]
CN
GELATIN,ABSORBABLE SPONGE
CN
GELATIN,ABSORBABLE SPONGE [VANDF]
CN
GELATINA [WHO-IP LATIN]
CN
GELATINE
CN
NDC Products Containing GELATIN, UNSPECIFIED
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 DrugCreon NDC 0032-1206
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugCreon NDC 0032-1212
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugCreon NDC 0032-1224
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugCreon NDC 0032-3016
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- BLA
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
NDC Product
Human Prescription DrugLupron Depot-ped NDC 0074-2108
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot-ped NDC 0074-2282
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot-ped NDC 0074-2440
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGengraf NDC 0074-3108
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGengraf NDC 0074-3109
- Generic Name
- Cyclosporine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot NDC 0074-3346
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot NDC 0074-3641
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot NDC 0074-3642
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot-ped NDC 0074-3779
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDepakote Sprinkles NDC 0074-6114
- Generic Name
- Divalproex Sodium
- Dosage Form
- Capsule
- 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
NDC Product
Human Prescription DrugLupron Depot-ped NDC 0074-9694
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- 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
E.R. Squibb & Sons, L.L.C.
NDC Product
Human Prescription DrugReyataz NDC 0003-3622
- Generic Name
- Atazanavir
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugReyataz NDC 0003-3631
- Generic Name
- Atazanavir
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugReyataz NDC 0003-3638
- Generic Name
- Atazanavir
- Dosage Form
- Powder
- Route
- Oral
- 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 Drug- Generic Name
- Dextromethorphan Hydrobromide And Guaifenesin
- Dosage Form
- Capsule, Liquid Filled
- 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 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 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
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 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 DrugBalsalazide Disodium NDC 0054-0079
- Generic Name
- Balsalazide Disodium
- Dosage Form
- Capsule
- 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 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 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 DrugLisdexamfetamine Dimesylate NDC 0054-0370
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0371
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0372
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0373
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0374
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0375
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- 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 DrugIcosapent Ethyl NDC 0054-0508
- Generic Name
- Icosapent Ethyl
- Dosage Form
- Capsule
- 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 DrugAlvimopan NDC 0054-0668
- Generic Name
- Alvimopan
- 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 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 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
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugEmend NDC 0006-0461
- Generic Name
- Aprepitant
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEmend NDC 0006-0462
- Generic Name
- Aprepitant
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEmend NDC 0006-0464
- Generic Name
- Aprepitant
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZolinza NDC 0006-0568
- Generic Name
- Vorinostat
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEmend NDC 0006-3066
- Generic Name
- Aprepitant
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEmend NDC 0006-3862
- Generic Name
- Aprepitant
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
VaccineProquad NDC 0006-4171
- Generic Name
- Measles, Mumps, Rubella And Varicella Virus Vaccine Live
- Dosage Form
- Injection, Powder, Lyophilized, For Suspension
- Route
- Intramuscular; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
VaccineM-m-r Ii NDC 0006-4681
- Generic Name
- Measles, Mumps, And Rubella Virus Vaccine Live
- Dosage Form
- Injection, Powder, Lyophilized, For Suspension
- Route
- Intramuscular; Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
VaccineVarivax NDC 0006-4827
- Generic Name
- Varicella Virus Vaccine Live
- Dosage Form
- Injection, Powder, Lyophilized, For Suspension
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1366
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1381
- Generic Name
- Temozolomide
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1417
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1425
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1430
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1519
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-3004
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- 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 DrugTasigna NDC 0078-0526
- Generic Name
- Nilotinib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTasigna NDC 0078-0592
- Generic Name
- Nilotinib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGilenya NDC 0078-0607
- Generic Name
- Fingolimod Hcl
- Dosage Form
- Capsule
- 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
NDC Product
Human Prescription DrugTasigna NDC 0078-0951
- Generic Name
- Nilotinib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGilenya NDC 0078-0965
- Generic Name
- Fingolimod Hcl
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFabhalta NDC 0078-1189
- Generic Name
- Iptacopan
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
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 DrugIbrance NDC 0069-0187
- Generic Name
- Palbociclib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIbrance NDC 0069-0188
- Generic Name
- Palbociclib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIbrance NDC 0069-0189
- Generic Name
- Palbociclib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSutent NDC 0069-0550
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSutent NDC 0069-0770
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSutent NDC 0069-0830
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSutent NDC 0069-0980
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugXalkori NDC 0069-8140
- Generic Name
- Crizotinib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugXalkori NDC 0069-8141
- Generic Name
- Crizotinib
- Dosage Form
- Capsule
- 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 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
Teva Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugDiclofenac Epolamine NDC 0093-3727
- Generic Name
- Diclofenac Epolamine
- Dosage Form
- System
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Teva Pharmaceuticals USA, Inc.
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 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
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 0093-1135
- 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
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 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
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 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 DrugAtomoxetine NDC 0093-3542
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3543
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3544
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3545
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3546
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3547
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3548
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylergonovine Maleate NDC 0093-3655
- Generic Name
- Methylergonovine Maleate
- Dosage Form
- Tablet
- 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 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
NDC Product
Human Prescription DrugAtazanavir Sulfate NDC 0093-5526
- Generic Name
- Atazanavir Sulfate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtazanavir Sulfate NDC 0093-5527
- Generic Name
- Atazanavir Sulfate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtazanavir Sulfate NDC 0093-5528
- Generic Name
- Atazanavir Sulfate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5550
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5551
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5552
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5553
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5554
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5562
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 0093-7163
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 0093-7164
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluoxetine NDC 0093-7198
- Generic Name
- Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0093-7334
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0093-7350
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0093-7351
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVenlafaxine Hydrochloride NDC 0093-7384
- Generic Name
- Venlafaxine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVenlafaxine Hydrochloride NDC 0093-7385
- Generic Name
- Venlafaxine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Viatris Specialty LLC
NDC Product
Human Prescription DrugDipentum NDC 0037-6860
- Generic Name
- Olsalazine Sodium
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
