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 |
---|---|---|---|---|---|
ACETAMINOPHEN; LIDOCAINE; ASPIRIN; BENZALKONIUM CHLORIDE; IBUPROFEN; ALCOHOL; BENZOCAINE | 52124-0118-1 | Genuine First Aid LLC | part333 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; NEOMYCIN SULFATE; ASPIRIN; SALICYLAMIDE; CAFFEINE; BACITRACIN ZINC; WATER; LIDOCAINE HYDROCHLORIDE; BENZALKONIUM CHLORIDE; CALCIUM CARBONATE; POLYMYXIN B SULFATE | 0498-4346-01 | Honeywell Safety Products USA, INC | HUMAN OTC DRUG | unapproved drug other | |
ACETAMINOPHEN; OXYCODONE | 10702-185-10 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE | 10702-184-10 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE | 10702-185-01 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE | 10702-184-01 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE | 10702-185-50 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE | 10702-184-50 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 68071-2856-3 | NuCare Pharmaceuticals,Inc. | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 67296-1815-9 | RedPharm Drug,Inc. | ANDA207419 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 53746-203-01 | Amneal Pharmaceuticals of New York LLC | ANDA040777 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 72022-582-01 | Halo Pharmaceutical Inc | ANDA207834 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 71335-2041-9 | Bryant Ranch Prepack | ANDA207419 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 47781-230-05 | Alvogen, Inc. | ANDA202677 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 67296-0522-4 | RedPharm Drug Inc. | ANDA040777 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 55700-498-90 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 68071-4852-2 | NuCare Pharmaceuticals,Inc. | ANDA207419 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 63187-721-30 | Proficient Rx LP | ANDA040778 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 63187-823-30 | Proficient Rx LP | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 70010-667-05 | Granules Pharmaceuticals Inc. | ANDA211708 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 55700-498-24 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 72245-193-03 | Forte Bio-Pharma LLC | ANDA040608 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 71335-1036-8 | Bryant Ranch Prepack | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 10544-287-50 | Blenheim Pharmacal, Inc. | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 71335-2041-8 | Bryant Ranch Prepack | ANDA207419 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 71205-486-30 | Proficient Rx LP | ANDA207419 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 68071-2932-2 | NuCare Pharmaceuticals,Inc. | ANDA201278 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 72865-114-05 | XLCare Pharmaceuticals, Inc. | ANDA207419 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 61919-871-60 | Direct_Rx | ANDA207419 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 31722-950-05 | Camber Pharmaceuticals, Inc. | ANDA207419 | HUMAN PRESCRIPTION DRUG | ANDA |
-