NDC Product
Human Prescription DrugTolterodine Tartrate NDC 50090-3475
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Hydroxypropyl Cellulose (110000 Wamw), uniquely identified by the FDA Unique Ingredient Identifier (UNII) 5Y0974F5PW.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-64-2 and the RxNorm Concept ID (RxCUI) 1485045. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
HYDROXYPROPYL CELLULOSE (110000 WAMW)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
5Y0974F5PW
The specific atomic composition represented as a molecular structure string.
Substance Type
polymer
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Hydroxypropyl Cellulose (110000 Wamw). Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.
Common Names & Synonyms
HYDROXYPROPYL CELLULOSE (110000 WAMW)
CN
HYDROXYPROPYL CELLULOSE (110000-150000 WAMW)
CN
HYDROXYPROPYL CELLULOSE (130000 WAMW)
CN
HYDROXYPROPYL CELLULOSE (200000 MW)
CN
HYDROXYPROPYL CELLULOSE L
CN
HYDROXYPROPYL CELLULOSE LF
CN
HYDROXYPROPYL CELLULOSE NF 75-150 CPS
CN
Brand / Trade Names
KLUCEL LF
BN
KLUCEL LXF
BN
NISSO HPC LM
BN
Technical Codes
YJL324Y3EQ
CD
NDC Products Containing HYDROXYPROPYL CELLULOSE (110000 WAMW)
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
A-S Medication Solutions
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil And Hydrochlorothiazide NDC 50090-3561
- Generic Name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil And Hydrochlorothiazide NDC 50090-3701
- Generic Name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil And Hydrochlorothiazide NDC 50090-4377
- Generic Name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSimvastatin NDC 50090-4897
- Generic Name
- Simvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-5181
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-5182
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-5184
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-5207
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-5208
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 50090-5918
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-6061
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 50090-6179
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 50090-6313
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 50090-6315
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 50090-6418
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVarenicline NDC 50090-6446
- Generic Name
- Varenicline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVarenicline NDC 50090-6447
- Generic Name
- Varenicline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 50090-7263
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7358
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7359
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7384
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7385
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7386
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7387
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 50090-7469
- Generic Name
- Potassium Chloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 50090-7498
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 50090-7499
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 50090-7513
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7528
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7529
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7532
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7533
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7574
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7575
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoprolol Succinate NDC 50090-7590
- Generic Name
- Metoprolol Succinate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoprolol Succinate NDC 50090-7591
- Generic Name
- Metoprolol Succinate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7806
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 50090-7807
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
AAA PHARMACEUTICAL, INC.
NDC Product
Human Otc DrugMigraine Relief NDC 57344-205
- Generic Name
- Acetaminophen, Aspirin And Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Accord Healthcare Inc.
NDC Product
Human Prescription DrugTeriflunomide NDC 16729-399
- Generic Name
- Teriflunomide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTeriflunomide NDC 16729-400
- Generic Name
- Teriflunomide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugBudesonide NDC 0591-2510
- Generic Name
- Budesonide
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Inc.
NDC Product
Human Prescription DrugMidodrine Hydrochloride NDC 62332-338
- Generic Name
- Midodrine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMidodrine Hydrochloride NDC 62332-339
- Generic Name
- Midodrine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMidodrine Hydrochloride NDC 62332-340
- Generic Name
- Midodrine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCandesartan Cilexetil NDC 62332-341
- Generic Name
- Candesartan Cilexetil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCandesartan Cilexetil NDC 62332-342
- Generic Name
- Candesartan Cilexetil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCandesartan Cilexetil NDC 62332-343
- Generic Name
- Candesartan Cilexetil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Limited
NDC Product
Human Prescription DrugMidodrine Hydrochloride NDC 46708-338
- Generic Name
- Midodrine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMidodrine Hydrochloride NDC 46708-339
- Generic Name
- Midodrine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMidodrine Hydrochloride NDC 46708-340
- Generic Name
- Midodrine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCandesartan Cilexetil NDC 46708-341
- Generic Name
- Candesartan Cilexetil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCandesartan Cilexetil NDC 46708-342
- Generic Name
- Candesartan Cilexetil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCandesartan Cilexetil NDC 46708-343
- Generic Name
- Candesartan Cilexetil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Apotex Corp
NDC Product
Human Prescription DrugVarenicline NDC 60505-3613
- Generic Name
- Varenicline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVarenicline NDC 60505-3614
- Generic Name
- Varenicline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurobindo Pharma Limited
NDC Product
Human Prescription DrugDarunavir NDC 59651-085
- Generic Name
- Darunavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDarunavir NDC 59651-086
- Generic Name
- Darunavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFebuxostat NDC 59651-113
- Generic Name
- Febuxostat
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFebuxostat NDC 59651-114
- Generic Name
- Febuxostat
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMontelukast Sodium NDC 59651-329
- Generic Name
- Montelukast Sodium
- Dosage Form
- Granule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEtyqa NDC 59651-424
- Generic Name
- Estradiol And Norethindrone Acetate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEtyqa NDC 59651-425
- Generic Name
- Estradiol And Norethindrone Acetate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 59651-456
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 59651-457
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 59651-458
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEsomeprazole Magnesium NDC 59651-802
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEsomeprazole Magnesium NDC 59651-803
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEsomeprazole Magnesium NDC 59651-804
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEsomeprazole Magnesium NDC 59651-805
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIbuprofen And Famotidine NDC 59651-908
- Generic Name
- Ibuprofen And Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurohealth LLC
NDC Product
Human Otc DrugAcetaminophen And Diphenhydramine Hydrochloride NDC 58602-760
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugCetirizine Hydrochloride NDC 58602-838
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Cetirizine Hydrochloride NDC 58602-856
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugCetirizine Hydrochloride NDC 58602-860
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugCetirizine Hydrochloride NDC 58602-862
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvPAK
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 50268-037
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 50268-038
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 50268-039
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 50268-040
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 50268-041
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Better Living Brands, LLC
NDC Product
Human Otc DrugAcetaminophen And Diphenhydramine Hydrochloride NDC 21130-224
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugFelodipine NDC 63629-2016
- Generic Name
- Felodipine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFelodipine NDC 63629-2017
- Generic Name
- Felodipine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFelodipine NDC 63629-2018
- Generic Name
- Felodipine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 63629-4134
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSimvastatin NDC 63629-7421
- Generic Name
- Simvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
CVS Pharmacy
NDC Product
Human Otc DrugGuaifenesin 600 Mg NDC 51316-008
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
CVS Pharmacy, Inc.
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugFluvoxamine Maleate NDC 31722-064
- Generic Name
- Fluvoxamine Maleate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluvoxamine Maleate NDC 31722-065
- Generic Name
- Fluvoxamine Maleate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cardinal Health 107, LLC
NDC Product
Human Prescription DrugLansoprazole NDC 55154-4848
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Carlsbad Technology, Inc.
NDC Product
Human Prescription DrugFelodipine NDC 61442-431
- Generic Name
- Felodipine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFelodipine NDC 61442-432
- Generic Name
- Felodipine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFelodipine NDC 61442-433
- Generic Name
- Felodipine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
DISCOUNT DRUG MART
NDC Product
Human Otc DrugMigraine Relief NDC 53943-305
- Generic Name
- Acetaminophen, Aspirin And Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dr. Reddy's Laboratories Inc.
NDC Product
Drug For Further Processing- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Otc DrugGuaifenesin 600 Mg NDC 43598-008
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin 1200 Mg NDC 43598-009
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Otc DrugGuaifenesin 1200 Mg NDC 43598-108
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin 600 Mg NDC 43598-110
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine NDC 43598-164
- Generic Name
- Olanzapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine NDC 43598-165
- Generic Name
- Olanzapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine NDC 43598-166
- Generic Name
- Olanzapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dr. Reddy's Laboratories Ltd.
NDC Product
Human Prescription DrugOlanzapine NDC 55111-167
- Generic Name
- Olanzapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine NDC 55111-168
- Generic Name
- Olanzapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
FAMILY DOLLAR
NDC Product
Human Otc DrugFamotidine NDC 55319-408
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugFamotidine NDC 55319-409
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen, Aspirin And Caffeine NDC 55319-680
- Generic Name
- Acetaminophen, Aspirin And Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
GERI-CARE PHARMACEUTICAL CORP
NDC Product
Human Otc DrugFamotidine NDC 57896-317
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Geri-Care Pharmaceutical Corp
NDC Product
Human Otc DrugFamotidine NDC 57896-319
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Golden State Medical Supply, Inc.
NDC Product
Human Prescription DrugFelodipine NDC 51407-088
- Generic Name
- Felodipine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFelodipine NDC 51407-089
- Generic Name
- Felodipine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSevelamer Carbonate NDC 51407-706
- Generic Name
- Sevelamer Carbonate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZileuton NDC 51407-741
- Generic Name
- Zileuton
- Dosage Form
- Tablet, Multilayer, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVarenicline NDC 51407-755
- Generic Name
- Varenicline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVarenicline NDC 51407-756
- Generic Name
- Varenicline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Granules India Ltd
NDC Product
Human Prescription DrugMetoprolol Succinate NDC 62207-130
- Generic Name
- Metoprolol Succinate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoprolol Succinate NDC 62207-131
- Generic Name
- Metoprolol Succinate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoprolol Succinate NDC 62207-132
- Generic Name
- Metoprolol Succinate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoprolol Succinate NDC 62207-133
- Generic Name
- Metoprolol Succinate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen, Aspirin And Caffeine NDC 62207-680
- Generic Name
- Acetaminophen, Aspirin And Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 62207-914
- Generic Name
- Potassium Chloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 62207-915
- Generic Name
- Potassium Chloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
KROGER COMPANY
NDC Product
Human Otc DrugCetirizine Hydrochloride NDC 30142-058
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen Extra Strength NDC 30142-165
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen And Diphenhydramine Hydrochloride NDC 30142-193
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Lannett Company, Inc.
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0527-4116
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0527-4117
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0527-4118
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0527-4119
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Micro Labs Limited
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 42571-333
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 42571-334
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibric Acid NDC 42571-347
- Generic Name
- Fenofibric Acid
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibric Acid NDC 42571-348
- Generic Name
- Fenofibric Acid
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRamelteon NDC 42571-375
- Generic Name
- Ramelteon
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugPotassium Chloride NDC 0615-8442
- Generic Name
- Potassium Chloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northstar Rx LLC.
NDC Product
Human Prescription DrugPhytonadione NDC 16714-973
- Generic Name
- Phytonadione
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northwind Health Company, LLC
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 51655-464
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 51655-465
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSimvastatin NDC 51655-598
- Generic Name
- Simvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSimvastatin NDC 51655-643
- Generic Name
- Simvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 51655-747
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 51655-946
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
PUBLIX SUPER MARKETS INC
NDC Product
Human Otc DrugPublix Super Markets Inc NDC 56062-305
- Generic Name
- Acetaminophen, Aspirin And Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Proficient Rx LP
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 63187-952
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
QPharma, Inc.
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 42708-003
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 42708-004
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 42708-005
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 42708-141
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 42708-144
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSimvastatin NDC 42708-148
- Generic Name
- Simvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rugby Laboratories
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
SAFEWAY
NDC Product
Human Otc DrugFamotidine NDC 21130-191
- Generic Name
- Famotidine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
ST. MARY'S MEDICAL PARK PHARMACY
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 60760-556
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 60760-882
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 60760-883
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 60760-907
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safeway, Inc
NDC Product
Human Otc DrugAcetaminophen, Aspirin And Caffeine NDC 21130-681
- Generic Name
- Acetaminophen, Aspirin And Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sun Pharmaceutical Industries, Inc.
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 62756-071
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
TWIN MED LLC
NDC Product
Human Otc DrugFamotidine NDC 55681-341
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugFamotidine NDC 55681-342
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals USA, Inc.
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
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0093-5056
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0093-5057
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0093-5058
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0093-5059
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 0093-5571
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 0093-5572
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- 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
Human Prescription DrugTolterodine Tartrate NDC 0093-7164
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Torrent Pharmaceuticals Limited
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
TruPharma, LLC
NDC Product
Human Prescription DrugRamelteon NDC 52817-235
- Generic Name
- Ramelteon
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Unichem Pharmaceuticals (USA), Inc.
NDC Product
Human Prescription DrugLacosamide NDC 29300-364
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 29300-365
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 29300-366
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 29300-367
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 29300-419
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 29300-420
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 29300-421
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 29300-422
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 29300-423
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 29300-424
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREEN CO
NDC Product
Human Otc DrugAcetaminophen Aspirin Caffeine NDC 0363-9680
- Generic Name
- Acetaminophen Aspirin Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREEN CO.
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugCetirizine Hydrochloride NDC 0363-0471
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Cetirizine Hydrochloride NDC 0363-4025
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
