NDC Product
Human Prescription DrugFamotidine NDC 50090-1044
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Polyethylene Glycol 3000, uniquely identified by the FDA Unique Ingredient Identifier (UNII) SA1B764746.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 25322-68-3 and the RxNorm Concept ID (RxCUI) 1368866. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
POLYETHYLENE GLYCOL 3000
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
SA1B764746
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 Polyethylene Glycol 3000. 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
PEG-60
OF
Common Names & Synonyms
MACROGOL 3000
CN
PEG 3000
CN
POLYETHYLENE GLYCOL 3000
CN
POLYETHYLENE GLYCOL 3000 [USP-RS]
CN
POLYOXYETHYLENE (60)
CN
Brand / Trade Names
POLYGLYKOL 3000
BN
NDC Products Containing POLYETHYLENE GLYCOL 3000
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 (181), only Active Listings are currently displayed.
Showing 123 active products
A-S Medication Solutions
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 50090-2007
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevonest NDC 50090-2505
- Generic Name
- Levonorgestrel And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 50090-4861
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFamotidine NDC 50090-6932
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
ANI Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugPrucalopride NDC 70954-596
- Generic Name
- Prucalopride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrucalopride NDC 70954-597
- Generic Name
- Prucalopride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugClarithromycin NDC 0591-2805
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Inc.
NDC Product
Human Prescription DrugFebuxostat NDC 62332-190
- Generic Name
- Febuxostat
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFebuxostat NDC 62332-191
- Generic Name
- Febuxostat
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlbendazole NDC 62332-681
- Generic Name
- Albendazole
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 62332-755
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 62332-756
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 62332-757
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 62332-758
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 62332-759
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 62332-760
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 62332-761
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 62332-762
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 62332-763
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 62332-764
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 62332-765
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Limited
NDC Product
Human Prescription DrugFebuxostat NDC 46708-190
- Generic Name
- Febuxostat
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFebuxostat NDC 46708-191
- Generic Name
- Febuxostat
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlbendazole NDC 46708-681
- Generic Name
- Albendazole
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 46708-755
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 46708-756
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 46708-757
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 46708-758
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 46708-759
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 46708-760
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 46708-761
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 46708-762
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 46708-763
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 46708-764
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 46708-765
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
American Health Packaging
NDC Product
Human Prescription DrugDivalproex Sodium NDC 60687-857
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 60687-868
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 60687-879
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amneal Pharmaceuticals LLC
NDC Product
Human Prescription DrugSpironolactone NDC 65162-514
- Generic Name
- Spironolactone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 65162-515
- Generic Name
- Spironolactone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugSpironolactone NDC 53746-514
- Generic Name
- Spironolactone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 53746-515
- Generic Name
- Spironolactone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurobindo Pharma Limited
NDC Product
Human Prescription DrugIrbesartan And Hydrochlorothiazide NDC 65862-629
- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugIrbesartan And Hydrochlorothiazide NDC 65862-630
- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan And Hydrochlorothiazide NDC 65862-631
- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
BluePoint Laboratories
NDC Product
Human Prescription DrugDivalproex Sodium NDC 68001-472
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 68001-473
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 68001-474
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugDivalproex Sodium NDC 63629-4278
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 63629-5241
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan And Hydrochlorothiazide NDC 63629-7468
- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 63629-8259
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71335-0008
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 71335-1263
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71335-2124
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71335-2862
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71335-2885
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 72162-2460
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugAmlodipine And Olmesartan Medoxomil NDC 31722-445
- Generic Name
- Amlodipine And Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Olmesartan Medoxomil NDC 31722-446
- Generic Name
- Aamlodipine And Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Olmesartan Medoxomil NDC 31722-447
- Generic Name
- Amlodipine And Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Olmesartan Medoxomil NDC 31722-448
- Generic Name
- Amlodipine And Olmesartan Medoxomil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cipla USA Inc.
NDC Product
Human Prescription DrugPrucalopride NDC 69097-218
- Generic Name
- Prucalopride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrucalopride NDC 69097-219
- Generic Name
- Prucalopride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
DirectRx
NDC Product
Human Prescription DrugDivalproex Sodium NDC 61919-249
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Ingenus Pharmaceuticals, LLC
NDC Product
Human Prescription DrugDolishale NDC 50742-659
- Generic Name
- Levonorgestrel And Ethinyl Estradiol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Janssen Products, LP
NDC Product
Human Prescription DrugEdurant NDC 59676-278
- Generic Name
- Rilpivirine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Kungpo Health Care & Herbal Center Inc
NDC Product
Human Otc DrugOra Yogu 4x Medicated Tooth And Gum Pain Reliever NDC 87351-761
- Generic Name
- Medicated Tooth And Gum Pain Reliever
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Lupin Pharmaceuticals,Inc.
NDC Product
Human Prescription DrugTinidazole NDC 43386-550
- Generic Name
- Tinidazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTinidazole NDC 43386-551
- Generic Name
- Tinidazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Macleods Pharmaceuticals Limited
NDC Product
Human Prescription DrugIrbesartan NDC 33342-047
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 33342-048
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 33342-049
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan And Hydrochlorothiazide NDC 33342-057
- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan And Hydrochlorothiazide NDC 33342-058
- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NorthStar RxLLC
NDC Product
Human Prescription DrugIrbesartan NDC 72603-670
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 72603-671
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 72603-672
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northstar Rx LLC
NDC Product
Human Prescription DrugLevonest NDC 16714-340
- Generic Name
- Levonorgestrel And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPimtrea NDC 16714-404
- Generic Name
- Desogestrel/ethinyl Estradiol And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
Northwind Health Company, LLC
NDC Product
Human Prescription DrugFamotidine NDC 51655-233
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 51655-365
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugCaduet NDC 0069-2260
- Generic Name
- Amlodipine Besylate And Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Prasco Laboratories
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 66993-263
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 66993-264
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 66993-265
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 66993-266
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 66993-267
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 66993-268
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 66993-269
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 66993-270
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 66993-271
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 66993-272
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 66993-273
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Proficient Rx LP
NDC Product
Human Prescription DrugIrbesartan And Hydrochlorothiazide NDC 63187-653
- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 63187-737
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 63187-742
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 63187-743
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFamotidine NDC 71205-276
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 71205-379
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
REMEDYREPACK INC.
NDC Product
Human Prescription DrugDivalproex Sodium NDC 70518-2626
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 70518-4575
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sandoz Inc.
NDC Product
Human Prescription DrugPrucalopride NDC 0781-8158
- Generic Name
- Prucalopride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrucalopride NDC 0781-8159
- Generic Name
- Prucalopride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Somerset Therapeutics, LLC
NDC Product
Human Prescription DrugRilpivirine NDC 70069-848
- Generic Name
- Rilpivirine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugFamotidine NDC 0172-5728
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFamotidine NDC 0172-5729
- Generic Name
- Famotidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Unichem Pharmaceuticals (USA), Inc.
NDC Product
Human Prescription DrugDivalproex Sodium NDC 29300-138
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 29300-139
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 29300-140
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Viatris Specialty LLC
NDC Product
Human Prescription DrugCaduet NDC 58151-062
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCaduet NDC 58151-063
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCaduet NDC 58151-065
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCaduet NDC 58151-066
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCaduet NDC 58151-067
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
