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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DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN | 59726-201-48 | P & L Development, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 59726-050-24 | P & L Development, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 59726-842-24 | P & L Development, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 59726-850-48 | P & L Development, LLC | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 49580-0335-9 | P & L Development, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; DOXYLAMINE SUCCINATE; DEXTROMETHORPHAN HYDROBROMIDE | 49580-0343-6 | P & L Development, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 59726-494-50 | P & L Development, LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 59726-031-15 | P & L Development, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 59726-447-24 | P & L Development, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE | 59726-028-48 | P & L Development, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE | 59726-028-24 | P & L Development, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 49580-0282-2 | P & L Development, LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 59726-198-24 | P & L Development, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 49580-0467-2 | P & L Development, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 45802-201-26 | Padagis Israel Pharmaceuticals Ltd | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 45802-730-00 | Padagis Israel Pharmaceuticals Ltd | ANDA070608 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 45802-730-30 | Padagis Israel Pharmaceuticals Ltd | ANDA070608 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 45802-203-26 | Padagis Israel Pharmaceuticals Ltd | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 45802-730-32 | Padagis Israel Pharmaceuticals Ltd | ANDA070608 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 45802-730-33 | Padagis Israel Pharmaceuticals Ltd | ANDA070608 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 45802-732-30 | Padagis Israel Pharmaceuticals Ltd | ANDA070607 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 45802-732-33 | Padagis Israel Pharmaceuticals Ltd | ANDA070607 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 0121-0966-94 | PAI Holdings, LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 0121-0941-05 | PAI Holdings, LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 0121-1882-11 | PAI Holdings, LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 0121-1781-00 | PAI Holdings, LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 0121-1544-40 | PAI Holdings, LLC | ANDA040838 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 0121-1008-00 | PAI Holdings, LLC | ANDA087508 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 0121-1544-10 | PAI Holdings, LLC | ANDA040838 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 0121-4772-05 | PAI Holdings, LLC | ANDA040838 | HUMAN PRESCRIPTION DRUG | ANDA |
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