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 | 54859-809-16 | LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43386-492-10 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 43386-353-01 | Lupin Pharmaceuticals,Inc. | ANDA206142 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 43386-358-03 | Lupin Pharmaceuticals,Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 43386-351-01 | Lupin Pharmaceuticals,Inc. | ANDA206142 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 43386-352-05 | Lupin Pharmaceuticals,Inc. | ANDA206142 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 43386-490-01 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 43386-353-03 | Lupin Pharmaceuticals,Inc. | ANDA206142 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 43386-356-05 | Lupin Pharmaceuticals,Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 43386-493-10 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43386-491-01 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 43386-357-10 | Lupin Pharmaceuticals,Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43386-492-01 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 43386-490-10 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 43386-493-01 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 43386-353-05 | Lupin Pharmaceuticals,Inc. | ANDA206142 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 43386-493-05 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 43386-490-05 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43386-491-05 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43386-491-10 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 43386-356-03 | Lupin Pharmaceuticals,Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 43386-357-01 | Lupin Pharmaceuticals,Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 43386-352-03 | Lupin Pharmaceuticals,Inc. | ANDA206142 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 43386-356-10 | Lupin Pharmaceuticals,Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 43386-351-05 | Lupin Pharmaceuticals,Inc. | ANDA206142 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 43386-356-01 | Lupin Pharmaceuticals,Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 43386-352-01 | Lupin Pharmaceuticals,Inc. | ANDA206142 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 43386-358-10 | Lupin Pharmaceuticals,Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 43386-357-03 | Lupin Pharmaceuticals,Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 43386-351-03 | Lupin Pharmaceuticals,Inc. | ANDA206142 | HUMAN PRESCRIPTION DRUG | ANDA |
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