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; OXYCODONE HYDROCHLORIDE | 71335-9675-6 | Bryant Ranch Prepack | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43598-547-01 | Dr. ReddyÂ’s Laboratories Inc. | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-1855-7 | Redpharm Drug, Inc | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 71335-9674-7 | Bryant Ranch Prepack | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 72189-255-30 | DIRECT RX | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 63629-1942-1 | Bryant Ranch Prepack | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 71930-045-12 | Eywa Pharma Inc | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 71335-9675-7 | Bryant Ranch Prepack | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43598-546-05 | Dr. ReddyÂ’s Laboratories Inc. | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 13107-211-05 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 13107-213-99 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 13107-213-05 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 13107-212-99 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 13107-212-05 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 13107-211-30 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 13107-213-30 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 13107-211-99 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 13107-212-01 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 13107-211-01 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 13107-213-01 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 13107-212-30 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 72022-582-01 | Halo Pharmaceutical Inc | ANDA207834 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 72022-582-05 | Halo Pharmaceutical Inc | ANDA207834 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 72022-584-05 | Halo Pharmaceutical Inc | ANDA207834 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 72022-583-05 | Halo Pharmaceutical Inc | ANDA207834 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 72022-584-01 | Halo Pharmaceutical Inc | ANDA207834 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 72022-583-01 | Halo Pharmaceutical Inc | ANDA207834 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 10702-193-01 | KVK-Tech, Inc. | ANDA209036 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 10702-193-10 | KVK-Tech, Inc. | ANDA209036 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 10702-192-50 | KVK-Tech, Inc. | ANDA209036 | HUMAN PRESCRIPTION DRUG | ANDA |
-