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; HYDROCODONE BITARTRATE | 67296-0016-2 | RedPharm Drug Inc. | ANDA081083 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 50090-0006-2 | A-S Medication Solutions | ANDA085055 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 63304-562-05 | Sun Pharmaceutical Industries, Inc. | ANDA085868 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 63304-562-10 | Sun Pharmaceutical Industries, Inc. | ANDA085868 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 63304-562-01 | Sun Pharmaceutical Industries, Inc. | ANDA085868 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 0054-4650-25 | West-Ward Pharmaceuticals Corp | ANDA087003 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 0054-4650-29 | West-Ward Pharmaceuticals Corp | ANDA087003 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 0054-8650-24 | West-Ward Pharmaceuticals Corp | ANDA087003 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 63304-561-05 | Sun Pharmaceutical Industries, Inc. | ANDA087083 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 63304-561-01 | Sun Pharmaceutical Industries, Inc. | ANDA087083 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 0406-0512-91 | SpecGx LLC | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 10544-287-50 | Blenheim Pharmacal, Inc. | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 10544-287-15 | Blenheim Pharmacal, Inc. | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 10544-287-06 | Blenheim Pharmacal, Inc. | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-0355-9 | RedPharm Drug, Inc. | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 0406-0512-05 | SpecGx LLC | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 49999-852-40 | Quality Care products LLC | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-0355-8 | RedPharm Drug, Inc. | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-0355-6 | RedPharm Drug, Inc. | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-0355-1 | RedPharm Drug, Inc. | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 10544-287-20 | Blenheim Pharmacal, Inc. | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 49999-852-14 | Quality Care products LLC | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 49999-852-15 | Quality Care products LLC | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 49999-852-60 | Quality Care products LLC | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 0406-0512-62 | SpecGx LLC | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 49999-852-00 | Quality Care products LLC | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 0406-0512-23 | SpecGx LLC | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-0355-3 | RedPharm Drug, Inc. | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-0355-5 | RedPharm Drug, Inc. | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-0355-4 | RedPharm Drug, Inc. | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
-