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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ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 50436-2983-2 | Unit Dose Services | ANDA201447 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 50436-3220-3 | Unit Dose Services | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; CODEINE PHOSPHATE | 50436-3227-1 | Unit Dose Services | ANDA040779 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 50436-3227-2 | Unit Dose Services | ANDA040779 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 50436-3227-7 | Unit Dose Services | ANDA040779 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 50436-3227-9 | Unit Dose Services | ANDA040779 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; CAFFEINE; ACETAMINOPHEN | 50436-3369-1 | Unit Dose Services | ANDA088616 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 50436-3913-1 | Unit Dose Services | ANDA201447 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 50436-3913-2 | Unit Dose Services | ANDA201447 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 50436-3913-3 | Unit Dose Services | ANDA201447 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 50436-3913-5 | Unit Dose Services | ANDA201447 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 50436-3918-1 | Unit Dose Services | ANDA090118 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 50436-3918-2 | Unit Dose Services | ANDA090118 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 50436-3918-4 | Unit Dose Services | ANDA090118 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 50436-3918-5 | Unit Dose Services | ANDA090118 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 50436-3918-8 | Unit Dose Services | ANDA090118 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 50436-3918-9 | Unit Dose Services | ANDA090118 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; BUTALBITAL; ACETAMINOPHEN | 50436-4856-1 | Unit Dose Services | ANDA089175 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; BUTALBITAL; ACETAMINOPHEN | 50436-4856-2 | Unit Dose Services | ANDA089175 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 50436-6719-1 | Unit Dose Services | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 50580-170-01 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 50580-170-02 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 50580-170-03 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 50580-170-04 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 50580-177-08 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 50580-194-01 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; IBUPROFEN | 50580-208-02 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 50580-208-08 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 50580-208-12 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 50580-208-16 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
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