FDA Application
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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 |
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OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 13107-045-30 | Aurolife Pharma, LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 13107-060-05 | Aurolife Pharma, LLC | ANDA202800 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 13107-211-05 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 13107-060-30 | Aurolife Pharma, LLC | ANDA202800 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 13107-020-01 | Aurolife Pharma, LLC | ANDA201013 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 13107-045-05 | Aurolife Pharma, LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 13107-044-30 | Aurolife Pharma, LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 13107-046-01 | Aurolife Pharma, LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 13107-046-99 | Aurolife Pharma, LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 13107-059-05 | Aurolife Pharma, LLC | ANDA202800 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 13107-212-99 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 13107-043-30 | Aurolife Pharma, LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 13107-021-99 | Aurolife Pharma, LLC | ANDA201013 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 13107-213-05 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 13107-058-05 | Aurolife Pharma, LLC | ANDA202800 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 13107-020-99 | Aurolife Pharma, LLC | ANDA201013 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 13107-213-99 | Aurolife Pharma, LLC | ANDA207709 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 63548-2341-1 | Avema Pharma Solutions | HUMAN OTC DRUG | Unapproved drug other | |
ASPIRIN; ACETAMINOPHEN; CAFFEINE | 69189-5135-1 | Avera McKennan Hospital | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
BUTALBITAL; CAFFEINE; ACETAMINOPHEN | 42291-181-01 | AvKARE | ANDA040885 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; ACETAMINOPHEN; CAFFEINE | 50268-553-13 | AvPAK | ANDA209587 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 50268-644-11 | AvPAK | ANDA040777 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 50268-401-15 | AvPAK | ANDA040736 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE | 50268-774-15 | AvPAK | ANDA090485 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE | 50268-774-11 | AvPAK | ANDA090485 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 50268-400-11 | AvPAK | ANDA040746 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 50268-645-11 | AvPAK | ANDA040778 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 50268-646-15 | AvPAK | ANDA040778 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 50268-646-11 | AvPAK | ANDA040778 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 50268-052-11 | AvPAK | ANDA076200 | HUMAN OTC DRUG | ANDA |
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