NDC Product
Human Prescription DrugDuloxetine NDC 0228-2890
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Hydroxypropyl Cellulose, Unspecified, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 9XZ8H6N6OH.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-64-2 and the RxNorm Concept ID (RxCUI) 1804020. 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, UNSPECIFIED
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
9XZ8H6N6OH
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
INN ID
7725
Sequential identifier assigned via the WHO International Nonproprietary Name program.
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 Hydroxypropyl Cellulose, 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
HYDROXYPROPYLCELLULOSE
OF
HYPROLOSE
OF
Common Names & Synonyms
CELLULOSE HYDROXYPROPYL ETHER
CN
CELLULOSE, 2-HYDROXYPROPYL ETHER
CN
HYDROXY PROPYL CELLULOSE
CN
HYDROXY PROPYL CELLULOSE NF
CN
HYDROXYPROPYL CELLULOSE
CN
HYDROXYPROPYL CELLULOSE [FCC]
CN
HYDROXYPROPYL CELLULOSE [II]
CN
HYDROXYPROPYL CELLULOSE [MI]
CN
HYDROXYPROPYL CELLULOSE [ORANGE BOOK]
CN
HYDROXYPROPYL CELLULOSE [USP-RS]
CN
HYDROXYPROPYL CELLULOSE [VANDF]
CN
HYDROXYPROPYL CELLULOSE NF
CN
HYDROXYPROPYL CELLULOSE, UNSPECIFIED
CN
HYDROXYPROPYLCELLULOSE [EP MONOGRAPH]
CN
HYDROXYPROPYLCELLULOSE [JAN]
CN
HYPROLOSE [INN]
CN
HYPROLOSE [WHO-DD]
CN
MODIFIED CELLULOSE
CN
Brand / Trade Names
LACRISERT
BN
Technical Codes
E-463
CD
INS NO.463
CD
INS-463
CD
NDC Products Containing HYDROXYPROPYL CELLULOSE, 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
Actavis Pharma, Inc.
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 0228-2891
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 0228-2892
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3090
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3091
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3092
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3093
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3116
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3117
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
AiPing Pharmaceutical, Inc.
NDC Product
Human Prescription DrugSevelamer Carbonate NDC 11788-116
- Generic Name
- Sevelamer Carbonate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Albertsons Companies
NDC Product
Human Otc DrugLansoprazole NDC 21130-046
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Astellas Pharma US, Inc.
NDC Product
Human Prescription DrugXospata NDC 0469-1425
- Generic Name
- Gilteritinib
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVeozah NDC 0469-2460
- Generic Name
- Fezolinetant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVeozah NDC 0469-2660
- Generic Name
- Fezolinetant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVeozah NDC 0469-2760
- Generic Name
- Fezolinetant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Aurolife Pharma LLC
NDC Product
Human Prescription DrugDiclofenac Sodium NDC 13107-269
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- ANDA
Active Listing
BETTER LIVING BRANDS LLC.
NDC Product
Human Otc DrugMaximum Strength Acid Controller NDC 21130-027
- Generic Name
- Famotidine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 21130-257
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen Diphenhydramine Hcl NDC 21130-354
- Generic Name
- Acetaminophen Diphenhydramine Hcl
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
BETTER LIVING BRANDS, LLC
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 21130-718
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bayer HealthCare LLC
NDC Product
Human Otc DrugTinactin Jock Itch NDC 11523-0138
- Generic Name
- Tolnaftate
- Dosage Form
- Aerosol, Powder
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bayer HealthCare LLC.
NDC Product
Human Otc DrugLotrimin Af Deodorant NDC 11523-0135
- Generic Name
- Miconazole Nitrate
- Dosage Form
- Aerosol, Powder
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLotrimin Daily Prevent Deodorant NDC 11523-0136
- Generic Name
- Tolnaftate
- Dosage Form
- Aerosol, Powder
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTinactin Deodorant NDC 11523-0137
- Generic Name
- Tolnaftate
- Dosage Form
- Aerosol, Powder
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTinactin NDC 11523-0139
- Generic Name
- Tolnaftate
- Dosage Form
- Aerosol, Powder
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bayer Healthcare LLC.
NDC Product
Human Otc DrugLotrimin Af NDC 11523-0134
- Generic Name
- Miconazole Nitrate
- Dosage Form
- Aerosol, Powder
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Better Living Brands LLC
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 21130-100
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen Extra Strength NDC 21130-155
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Carwin Pharmaceutical Associates, LLC
NDC Product
Human Prescription DrugOpipza NDC 15370-401
- Generic Name
- Aripiprazole
- Dosage Form
- Film, Soluble
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugOpipza NDC 15370-402
- Generic Name
- Aripiprazole
- Dosage Form
- Film, Soluble
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugOpipza NDC 15370-403
- Generic Name
- Aripiprazole
- Dosage Form
- Film, Soluble
- Route
- Oral
- Marketing
- NDA
Active Listing
Cosette Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugCalcipotriene NDC 0713-0318
- Generic Name
- Calcipotriene
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEvoxac NDC 0713-0883
- Generic Name
- Cevimeline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCevimeline Hydrochloride NDC 0713-0937
- Generic Name
- Cevimeline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Eli Lilly and Company
NDC Product
Human Prescription DrugInluriyo NDC 0002-1717
- Generic Name
- Imlunestrant
- Dosage Form
- Tablet, Film Coated
- 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 0004-0260
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Tablet, Film Coated
- 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
Haleon US Holdings LLC
NDC Product
Human Otc DrugExcedrin Extra Strength Pain Reliever NDC 0067-2001
- 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 Migraine Geltabs NDC 0067-2035
- Generic Name
- Acetaminophen, Asprin, Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine NDC 0067-2040
- Generic Name
- Acetaminophen, Aspirin, And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
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 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 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
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
NDC Product
Human Prescription DrugPerphenazine NDC 23155-799
- Generic Name
- Perphenazine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPerphenazine NDC 23155-800
- Generic Name
- Perphenazine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company Inc.
NDC Product
Human Prescription DrugBupropion Hydrochloride (xl) NDC 0527-2415
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride (xl) NDC 0527-2430
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company, Inc.
NDC Product
Human Prescription DrugOlmesartan Medoxomil NDC 0527-2425
- Generic Name
- Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil NDC 0527-2426
- Generic Name
- Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlmesartan Medoxomil NDC 0527-2427
- Generic Name
- Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugPosaconazole NDC 0904-7149
- Generic Name
- Posaconazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0904-7217
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0904-7218
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0904-7219
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0904-7220
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 0904-7244
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 0904-7245
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 0904-7246
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 0904-7247
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugLagevrio NDC 0006-5055
- Generic Name
- Molnupiravir
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- EMERGENCY USE AUTHORIZATION
Active Listing
NDC Product
Human Prescription DrugSteglujan NDC 0006-5367
- Generic Name
- Ertugliflozin And Sitagliptin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSteglujan NDC 0006-5368
- Generic Name
- Ertugliflozin And Sitagliptin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSegluromet NDC 0006-5369
- Generic Name
- Ertugliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSegluromet NDC 0006-5370
- Generic Name
- Ertugliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSegluromet NDC 0006-5373
- Generic Name
- Ertugliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSegluromet NDC 0006-5374
- Generic Name
- Ertugliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 0378-0088
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 0378-0094
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlordiazepoxide And Amitriptyline Hydrochloride NDC 0378-0211
- Generic Name
- Chlordiazepoxide And Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDabigatran Etexilate NDC 0378-0265
- Generic Name
- Dabigatran Etexilate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDabigatran Etexilate NDC 0378-0266
- Generic Name
- Dabigatran Etexilate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlordiazepoxide And Amitriptyline Hydrochloride NDC 0378-0277
- Generic Name
- Chlordiazepoxide And Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTeriflunomide NDC 0378-0627
- Generic Name
- Teriflunomide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTeriflunomide NDC 0378-0628
- Generic Name
- Teriflunomide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCandesartan Cilexetil NDC 0378-3224
- Generic Name
- Candesartan Cilexetil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCandesartan Cilexetil NDC 0378-3225
- Generic Name
- Candesartan Cilexetil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCandesartan Cilexetil NDC 0378-3231
- Generic Name
- Candesartan Cilexetil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCandesartan Cilexetil NDC 0378-3232
- Generic Name
- Candesartan Cilexetil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0378-3950
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0378-3951
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0378-3952
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0378-3953
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4513
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4514
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4515
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4516
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4517
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4518
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4519
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4520
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0378-6981
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0378-6982
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0378-7001
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0378-7002
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0378-7003
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0378-7004
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 0378-8085
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 0378-8086
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugMetoprolol Succinate NDC 0615-7823
- Generic Name
- Metoprolol Succinate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoprolol Succinate NDC 0615-7824
- Generic Name
- Metoprolol Succinate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetoprolol Succinate NDC 0615-7825
- Generic Name
- Metoprolol Succinate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPromethazine Hydrochloride NDC 0615-8154
- Generic Name
- Promethazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0615-8379
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0615-8380
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0615-8381
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 0615-8460
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 0615-8461
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 0615-8508
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 0615-8570
- Generic Name
- Potassium Chloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClopidogrel Bisulfate NDC 0615-8625
- Generic Name
- Clopidogrel Bisulfate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northstar Rx LLC.
NDC Product
Human Prescription DrugColchicine NDC 16714-039
- Generic Name
- Colchicine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlipizide NDC 16714-894
- Generic Name
- Glipizide
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlipizide NDC 16714-895
- Generic Name
- Glipizide
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlipizide NDC 16714-896
- Generic Name
- Glipizide
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugKisqali NDC 0078-0860
- Generic Name
- Ribociclib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugKisqali NDC 0078-0867
- Generic Name
- Ribociclib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugKisqali NDC 0078-0874
- Generic Name
- Ribociclib
- Dosage Form
- Tablet, Film Coated
- 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 DrugScemblix NDC 0078-1091
- Generic Name
- Asciminib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugScemblix NDC 0078-1098
- Generic Name
- Asciminib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Person and Covey
NDC Product
Human Otc DrugSolbar Thirty NDC 0096-0689
- Generic Name
- Sunscreen
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugGabapentin NDC 16571-117
- Generic Name
- Gabapentin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGabapentin NDC 16571-226
- Generic Name
- Gabapentin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 16571-880
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rite Aid
NDC Product
Human Otc DrugOmeprazole NDC 11822-0061
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rite Aid Corporation
NDC Product
Human Otc DrugLansoprazole NDC 11822-0019
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSleep-aid NDC 11822-0685
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rugby Laboratories
NDC Product
Human Otc DrugAcetaminophen NDC 0536-1292
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Coated Mint Flavor NDC 0536-3112
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Coated Mint Flavor NDC 0536-3113
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Coated Fruit Flavor NDC 0536-3386
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Coated Fruit Flavor NDC 0536-3387
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
Rugby Laboratories, Inc
NDC Product
Human Otc DrugLansoprazole NDC 0536-1368
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rugby Laboratories, Inc.
NDC Product
Human Otc DrugNicotine NDC 0536-1337
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMaxi Nicotine NDC 0536-1338
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safeway
NDC Product
Human Otc DrugIbuprofen Pm NDC 21130-623
- Generic Name
- Diphenhydramine Citrate, Ibuprofen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safeway, Inc.
NDC Product
Human Otc DrugHeadache Relief Extra Strength NDC 21130-586
- Generic Name
- Acetaminophen, Aspirin, Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEsomeprazole NDC 21130-926
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0781-5175
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPirfenidone NDC 0781-8085
- Generic Name
- Pirfenidone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPirfenidone NDC 0781-8086
- Generic Name
- Pirfenidone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
SpecGx LLC
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0803
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0804
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0805
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0807
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single Entity Amphetamine Product Xr NDC 0406-8951
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single Entity Amphetamine Product Xr NDC 0406-8952
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single Entity Amphetamine Product Xr NDC 0406-8953
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single Entity Amphetamine Product Xr NDC 0406-8954
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single Entity Amphetamine Product Xr NDC 0406-8955
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single Entity Amphetamine Product Xr NDC 0406-8956
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
TARGET CORPORATION
NDC Product
Human Otc DrugAcetaminophen NDC 11673-167
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMaximum Strength Acid Reducer NDC 11673-697
- Generic Name
- Famotidine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
TARGET Corporation
NDC Product
Human Otc DrugHeadache Relief Extra Strength NDC 11673-686
- Generic Name
- Acetaminophen, Aspirin, Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Target Corporation
NDC Product
Human Otc DrugLansoprazole NDC 11673-324
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugImatinib Mesylate NDC 0093-7629
- Generic Name
- Imatinib Mesylate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImatinib Mesylate NDC 0093-7630
- Generic Name
- Imatinib Mesylate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugFidaxomicin NDC 0480-2596
- Generic Name
- Fidaxomicin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTiopronin NDC 0480-7824
- Generic Name
- Tiopronin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTiopronin NDC 0480-9227
- Generic Name
- Tiopronin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Torrent Pharmaceuticals Limited
NDC Product
Human Prescription DrugTadalafil NDC 13668-565
- Generic Name
- Tadalafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 13668-566
- Generic Name
- Tadalafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 13668-567
- Generic Name
- Tadalafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 13668-568
- Generic Name
- Tadalafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 13668-581
- Generic Name
- Tadalafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 13668-586
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 13668-588
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 13668-606
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 13668-607
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTiopronin NDC 13668-691
- Generic Name
- Tiopronin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTiopronin NDC 13668-692
- Generic Name
- Tiopronin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Upsher-Smith Laboratories, LLC
NDC Product
Human Prescription DrugRamelteon NDC 0832-1250
- Generic Name
- Ramelteon
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREEN CO.
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 0363-0508
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0363-9798
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen Diphenhydramine Hcl NDC 0363-9799
- Generic Name
- Acetaminophen Diphenhydramine Hcl
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
WALGREENS
NDC Product
Human Otc DrugEsomeprazole Magnesium Delayed Release NDC 0363-7810
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREENS CO.
NDC Product
Human Otc DrugWalgreens Upset Stomach And Nausea Relief NDC 0363-1834
- Generic Name
- Sodium Citrate Dihydrate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugAcetaminophen Diphenhydramine Hcl NDC 0363-9664
- Generic Name
- Acetaminophen Diphenhydramine Hcl
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
WALGREENS COMPANY
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 0363-0772
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreen Company
NDC Product
Human Otc DrugPain Reliever Extra Strength NDC 0363-0519
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMulti-symptom Allergy NDC 0363-0559
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTension Headache Relief NDC 0363-0572
- Generic Name
- Acetaminophen, Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreens
NDC Product
Human Otc DrugNicotine NDC 0363-3911
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-5760
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugOmeprazole NDC 0363-9510
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-9620
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-9780
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens company
NDC Product
Human Otc DrugLansoprazole NDC 0363-0037
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
