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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OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-1855-3 | Redpharm Drug, Inc | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-1855-4 | Redpharm Drug, Inc | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-1855-5 | Redpharm Drug, Inc | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-1855-6 | Redpharm Drug, Inc | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-1855-7 | Redpharm Drug, Inc | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-1855-8 | Redpharm Drug, Inc | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 67296-1855-9 | Redpharm Drug, Inc | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE; ACETAMINOPHEN | 67296-1857-1 | Redpharm drug, inc | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE; ACETAMINOPHEN | 67296-1857-2 | Redpharm drug, inc | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE; ACETAMINOPHEN | 67296-1857-3 | Redpharm drug, inc | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE; ACETAMINOPHEN | 67296-1857-4 | Redpharm drug, inc | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE; ACETAMINOPHEN | 67296-1857-7 | Redpharm drug, inc | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE; ACETAMINOPHEN | 67296-1857-8 | Redpharm drug, inc | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 67296-1890-1 | Redpharm drug | ANDA040409 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 67296-1890-2 | RedPharm Drug, Inc | ANDA040409 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 67296-1890-3 | RedPharm Drug, Inc | ANDA040409 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 67296-1890-4 | RedPharm Drug, Inc | ANDA040409 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 67296-1890-6 | Redpharm drug | ANDA040409 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 67296-1890-7 | RedPharm Drug, Inc | ANDA040409 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 67296-1890-8 | RedPharm Drug, Inc | ANDA040409 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 67296-1890-9 | RedPharm Drug, Inc | ANDA040409 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 67296-1905-6 | Redpharm Drug | ANDA040405 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 67296-2093-1 | Redpharm drug | ANDA040838 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; ASPIRIN; ACETAMINOPHEN | 67414-239-02 | Jones Healthcare Group - Packaging Services, Inc | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; GUAIFENESIN | 67414-402-00 | Jones Healthcare Group - Packaging Services, Inc | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; GUAIFENESIN | 67414-402-02 | Jones Healthcare Group - Packaging Services, Inc | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 67414-449-00 | Jones Healthcare Group - Packaging Services, Inc | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 67414-449-10 | Jones Healthcare Group - Packaging Services, Inc | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 67414-449-11 | Jones Healthcare Group - Packaging Services, Inc | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; GUAIFENESIN | 67414-507-00 | Jones Healthcare Group - Packaging Services, Inc | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
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