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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HYDROCODONE BITARTRATE; ACETAMINOPHEN | 40032-353-03 | Novel Laboratories, Inc. | ANDA206142 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 40032-353-05 | Novel Laboratories, Inc. | ANDA206142 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 40032-356-01 | Novel Laboratories, Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 40032-356-03 | Novel Laboratories, Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 40032-356-05 | Novel Laboratories, Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 40032-356-10 | Novel Laboratories, Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 40032-357-01 | Novel Laboratories, Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 40032-357-03 | Novel Laboratories, Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 40032-357-05 | Novel Laboratories, Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 40032-357-10 | Novel Laboratories, Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 40032-358-01 | Novel Laboratories, Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 40032-358-03 | Novel Laboratories, Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 40032-358-05 | Novel Laboratories, Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 40032-358-10 | Novel Laboratories, Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
GUAIFENESIN; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE | 41163-035-06 | EQUALINE (SuperValu) | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 41163-045-08 | United Natural Foods, Inc. dba UNFI | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; GUAIFENESIN | 41163-053-08 | United Natural Foods, Inc. dba UNFI | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; IBUPROFEN | 41163-103-68 | United Natural Foods, Inc. dba UNFI | ANDA214836 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 41163-103-89 | United Natural Foods, Inc. dba UNFI | ANDA214836 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 41163-192-01 | United Natural Foods, Inc. dba UNFI | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 41163-203-02 | United Natural Foods, Inc. dba UNFI | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 41163-203-03 | United Natural Foods, Inc. dba UNFI | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 41163-214-10 | SuperValu (Equaline) | part338 | HUMAN OTC DRUG | OTC MONOGRAPH FINAL |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 41163-214-50 | SuperValu (Equaline) | part338 | HUMAN OTC DRUG | OTC MONOGRAPH FINAL |
DIPHENHYDRAMINE HYDROCHLORIDE; ACETAMINOPHEN | 41163-228-50 | United Natural Foods, Inc. dba UNFI | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
DIPHENHYDRAMINE HYDROCHLORIDE; ACETAMINOPHEN | 41163-229-50 | EQUALINE (SuperValu) | part338 | HUMAN OTC DRUG | OTC MONOGRAPH FINAL |
ACETAMINOPHEN | 41163-333-50 | SUPERVALU INC. | ANDA076200 | HUMAN OTC DRUG | ANDA |
CAFFEINE; ASPIRIN; ACETAMINOPHEN | 41163-334-08 | United Natural Foods, Inc. dba UNFI | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
CAFFEINE; ASPIRIN; ACETAMINOPHEN | 41163-334-12 | United Natural Foods, Inc. dba UNFI | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
DOXYLAMINE SUCCINATE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 41163-335-34 | United Natural Foods, Inc. dba UNFI | part341 | HUMAN OTC DRUG | OTC monograph final |
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