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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PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; DIPHENHYDRAMINE HYDROCHLORIDE; ACETAMINOPHEN; GUAIFENESIN | 11673-463-12 | TARGET Corporation | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 11673-484-52 | Target Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 11673-484-62 | Target Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 11673-484-71 | Target Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 11673-484-76 | Target Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 11673-484-78 | Target Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 11673-484-83 | Target Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 11673-484-85 | Target Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 11673-484-90 | Target Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE | 11673-500-40 | Target Corporation | part341 | HUMAN OTC DRUG | OTC monograph final |
DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; GUAIFENESIN | 11673-518-24 | TARGET Corporation | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 11673-519-12 | Target Corporation | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 11673-519-15 | Target Corporation | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 11673-519-20 | Target Corporation | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DIPHENHYDRAMINE HYDROCHLORIDE | 11673-542-12 | Target Corporation | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE | 11673-597-02 | Target Corporation | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 11673-618-62 | Target Corporation | ANDA075077 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 11673-618-78 | Target Corporation | ANDA075077 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 11673-673-01 | TARGET CORPORATION | ANDA215486 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 11673-673-26 | TARGET CORPORATION | ANDA215486 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; CAFFEINE; ASPIRIN | 11673-686-20 | TARGET Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; CAFFEINE; ASPIRIN | 11673-686-80 | TARGET Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE; TRIPROLIDINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 11673-691-12 | TARGET CORPORATION | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE | 11673-694-09 | Target Corporation | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
TRIPROLIDINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 11673-698-06 | TARGET CORPORATION | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DOXYLAMINE SUCCINATE | 11673-733-02 | Target Corporation | part341 | HUMAN OTC DRUG | OTC monograph final |
GUAIFENESIN; ACETAMINOPHEN; DOXYLAMINE SUCCINATE; DEXTROMETHORPHAN HYDROBROMIDE | 11673-739-02 | TARGET CORPORATION | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 11673-754-10 | TARGET Corporation | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; ACETAMINOPHEN | 11673-757-83 | TARGET CORPORATION | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 11673-759-26 | Target Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
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