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; OXYCODONE HYDROCHLORIDE | 72865-116-05 | XLCare Pharmaceuticals, Inc. | ANDA207419 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 72865-201-01 | XLCare Pharmaceuticals, Inc. | ANDA211487 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 72865-202-01 | XLCare Pharmaceuticals, Inc. | ANDA211487 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 72865-202-05 | XLCare Pharmaceuticals, Inc. | ANDA211487 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 72865-203-01 | XLCare Pharmaceuticals, Inc. | ANDA211487 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 72865-203-05 | XLCare Pharmaceuticals, Inc. | ANDA211487 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 72865-204-01 | XLCare Pharmaceuticals, Inc. | ANDA211487 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 72865-204-05 | XLCare Pharmaceuticals, Inc. | ANDA211487 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 72887-193-03 | FH2 Pharma LLC | ANDA040608 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 72887-648-12 | FH2 Pharma LLC | ANDA202142 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 72887-681-03 | FH2 Pharma LLC | ANDA040608 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 72887-682-03 | FH2 Pharma LLC | ANDA040608 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 72887-683-03 | FH2 Pharma LLC | ANDA040608 | HUMAN PRESCRIPTION DRUG | ANDA |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE | 72988-0027-1 | Lydia Co., Ltd. | HUMAN OTC DRUG | unapproved drug other | |
ACETAMINOPHEN; CAFFEINE | 72988-0032-1 | Lydia Co., Ltd. | HUMAN OTC DRUG | unapproved drug other | |
ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE | 72988-0033-1 | Lydia Co., Ltd. | HUMAN OTC DRUG | unapproved drug other | |
ACETAMINOPHEN; PROPYPHENAZONE | 72988-0036-1 | Lydia Co., Ltd. | HUMAN OTC DRUG | unapproved drug other | |
GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN | 73006-108-41 | O4 Global Trading Usa, Llc | part341 | HUMAN OTC DRUG | OTC monograph final |
CAFFEINE; ACETAMINOPHEN | 73006-110-41 | O4 Global Trading Usa, Llc | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 73006-117-41 | O4 Global Trading Usa, Llc | part343 | HUMAN OTC DRUG | OTC monograph not final |
DIPHENHYDRAMINE HYDROCHLORIDE; ACETAMINOPHEN | 73006-119-41 | O4 Global Trading Usa, Llc | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 73006-120-95 | O4 Global Trading Usa, Llc | part343 | HUMAN OTC DRUG | OTC monograph not final |
ASPIRIN; ACETAMINOPHEN; CAFFEINE | 73006-132-95 | O4 Global Trading Usa, Llc | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 73006-143-95 | O4 Global Trading Usa, Llc | part343 | HUMAN OTC DRUG | OTC monograph not final |
CAFFEINE; DIPHENHYDRAMINE HYDROCHLORIDE; ACETAMINOPHEN; ASPIRIN | 73006-350-98 | O4 Global Trading Usa, Llc | part338 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 73057-350-08 | Ulai Health LLC | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 73057-350-11 | Ulai Health LLC | part343 | HUMAN OTC DRUG | OTC monograph not final |
DIPHENHYDRAMINE HYDROCHLORIDE; ACETAMINOPHEN | 73057-352-03 | Ulai Health LLC | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 73057-353-08 | Ulai Health LLC | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 73057-353-11 | Ulai Health LLC | part343 | HUMAN OTC DRUG | OTC monograph not final |
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