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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GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 68016-628-20 | CHAIN DRUG CONSORTIUM | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68016-691-60 | Chain Drug Consortium | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; ACETAMINOPHEN | 68016-508-24 | CHAIN DRUG CONSORTIUM | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68016-502-50 | CHAIN DRUG CONSORTIUM | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 68016-543-01 | Chain Drug Consortium | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; CAFFEINE; PYRILAMINE MALEATE | 68016-736-24 | Chain Drug Consortium | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
PHENYLEPHRINE HYDROCHLORIDE; GUAIFENESIN; ACETAMINOPHEN | 68016-549-20 | CHAIN DRUG CONSORTIUM | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68016-502-00 | CHAIN DRUG CONSORTIUM | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 68016-303-01 | CHAIN DRUG CONSORTIUM | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 68016-198-00 | Chain Drug Consortium | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; GUAIFENESIN | 68016-625-20 | CHAIN DRUG CONSORTIUM | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68016-196-00 | Chain Drug Consortium | part343 | HUMAN OTC DRUG | OTC monograph not final |
PHENYLEPHRINE HYDROCHLORIDE; GUAIFENESIN; ACETAMINOPHEN | 68016-504-24 | CHAIN DRUG CONSORTIUM | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68016-734-50 | CHAIN DRUG CONSORTIUM | part343 | HUMAN OTC DRUG | OTC monograph not final |
GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 68016-717-24 | CHAIN DRUG CONSORTIUM | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68016-543-99 | Chain Drug Consortium | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 68016-503-03 | CHAIN DRUG CONSORTIUM | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 68016-541-01 | Chain Drug Consortium | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 68016-543-24 | Chain Drug Consortium | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 68016-734-22 | CHAIN DRUG CONSORTIUM | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 68016-303-50 | CHAIN DRUG CONSORTIUM | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 68016-691-01 | Chain Drug Consortium | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 68016-512-24 | CHAIN DRUG CONSORTIUM | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68016-734-01 | CHAIN DRUG CONSORTIUM | part343 | HUMAN OTC DRUG | OTC monograph not final |
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 68016-174-24 | CHAIN DRUG CONSORTIUM | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68016-160-02 | Chain Drug Consortium (Premier Value) | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
ACETAMINOPHEN | 68016-141-04 | Chain Drug Consortium (Premier Value) | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
ACETAMINOPHEN | 68016-103-04 | Chain Drug Consortium (Premier Value) | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
ACETAMINOPHEN | 68016-178-04 | Chain Drug Consortium (Premier Value) | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; ACETAMINOPHEN | 68016-135-00 | Chain Drug Consortium, LLC | part343 | HUMAN OTC DRUG | OTC monograph not final |
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