FDA Application
-
NDC Search Results on Active Ingredient: acetaminophen
Click on Active Ingredient to view the label.
Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
---|---|---|---|---|---|
ASPIRIN; CAFFEINE; ACETAMINOPHEN | 62207-680-98 | Granules India Ltd | ANDA214039 | HUMAN OTC DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 70010-674-05 | Granules Pharmaceuticals Inc. | ANDA211729 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 70010-667-05 | Granules Pharmaceuticals Inc. | ANDA211708 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 70010-672-01 | Granules Pharmaceuticals Inc. | ANDA211729 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; ACETAMINOPHEN | 70010-131-26 | Granules Pharmaceuticals Inc. | ANDA216592 | HUMAN OTC DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 70010-672-05 | Granules Pharmaceuticals Inc. | ANDA211729 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 70010-674-01 | Granules Pharmaceuticals Inc. | ANDA211729 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 70010-668-01 | Granules Pharmaceuticals Inc. | ANDA211708 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 70010-673-01 | Granules Pharmaceuticals Inc. | ANDA211729 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 70010-673-05 | Granules Pharmaceuticals Inc. | ANDA211729 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 70010-668-05 | Granules Pharmaceuticals Inc. | ANDA211708 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 70010-669-05 | Granules Pharmaceuticals Inc. | ANDA211708 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CAFFEINE; BUTALBITAL | 70010-149-05 | Granules Pharmaceuticals Inc. | ANDA040864 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 70010-161-05 | Granules Pharmaceuticals Inc. | HUMAN OTC DRUG | Export only | |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 70010-669-01 | Granules Pharmaceuticals Inc. | ANDA211708 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CAFFEINE; BUTALBITAL | 70010-149-01 | Granules Pharmaceuticals Inc. | ANDA040864 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; ACETAMINOPHEN | 70010-054-05 | Granules Pharmaceuticals Inc. | ANDA213115 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; ACETAMINOPHEN | 70010-054-01 | Granules Pharmaceuticals Inc. | ANDA213115 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 70010-670-01 | Granules Pharmaceuticals Inc. | ANDA211708 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 70010-667-01 | Granules Pharmaceuticals Inc. | ANDA211708 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 70010-160-01 | Granules Pharmaceuticals Inc. | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 70010-161-01 | Granules Pharmaceuticals Inc. | HUMAN OTC DRUG | Export only | |
ACETAMINOPHEN; BUTALBITAL; CAFFEINE | 70010-044-01 | Granules Pharmaceuticals Inc. | ANDA213321 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; ACETAMINOPHEN | 70010-131-31 | Granules Pharmaceuticals Inc. | ANDA216592 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 70010-161-10 | Granules Pharmaceuticals Inc. | HUMAN OTC DRUG | Export only | |
ACETAMINOPHEN; BUTALBITAL; CAFFEINE | 70010-044-05 | Granules Pharmaceuticals Inc. | ANDA213321 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 70010-670-05 | Granules Pharmaceuticals Inc. | ANDA211708 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 69848-003-24 | Granules USA, Inc | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 69848-003-10 | Granules USA, Inc | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 69848-008-10 | Granules USA, Inc | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
-