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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IBUPROFEN; ACETAMINOPHEN | 0573-0145-99 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 51672-2114-4 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 50580-783-10 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; BENZHYDROCODONE HYDROCHLORIDE | 10702-340-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN; IBUPROFEN | 67751-211-01 | Navajo Manufacturing Company Inc. | NDA211733 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; IBUPROFEN | 67751-211-02 | Navajo Manufacturing Company Inc. | NDA211733 | HUMAN OTC DRUG | NDA |
ASPIRIN; ACETAMINOPHEN; CAFFEINE | 0067-2039-07 | Haleon US Holdings LLC | NDA020802 | HUMAN OTC DRUG | NDA |
ASPIRIN; ACETAMINOPHEN; CAFFEINE | 0067-2039-24 | Haleon US Holdings LLC | NDA020802 | HUMAN OTC DRUG | NDA |
ASPIRIN; CAFFEINE; ACETAMINOPHEN | 66715-9749-3 | Lil' Drug Store Products, Inc. | NDA020802 | HUMAN OTC DRUG | NDA |
ASPIRIN; ACETAMINOPHEN; CAFFEINE | 0067-2040-03 | Haleon US Holdings LLC | NDA020802 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 51672-2116-2 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
IBUPROFEN; ACETAMINOPHEN | 0573-0145-02 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 50580-783-24 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 0143-9386-10 | Hikma Pharmaceuticals USA Inc. | NDA206968 | HUMAN PRESCRIPTION DRUG | NDA |
ASPIRIN; ACETAMINOPHEN; CAFFEINE | 0067-2040-02 | Haleon US Holdings LLC | NDA020802 | HUMAN OTC DRUG | NDA |
BENZHYDROCODONE HYDROCHLORIDE; ACETAMINOPHEN | 10702-343-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
BUTALBITAL; ACETAMINOPHEN; CAFFEINE; CODEINE PHOSPHATE | 0591-3220-01 | Actavis Pharma, Inc. | NDA020232 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
ACETAMINOPHEN; BENZHYDROCODONE HYDROCHLORIDE | 10702-345-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
BENZHYDROCODONE HYDROCHLORIDE; ACETAMINOPHEN | 10702-344-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
DIPHENHYDRAMINE HYDROCHLORIDE; ACETAMINOPHEN | 46122-643-71 | AmerisourceBergen (Good Neighbor Pharmacy) 46122 | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN | 79481-6300-8 | MEIJER DISTRIBUTION INC | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; GUAIFENESIN | 36800-035-06 | TOP CARE (Topco Associates LLC) | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 11673-241-24 | Target Corporation | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
PHENYLEPHRINE HYDROCHLORIDE; CHLORPHENIRAMINE MALEATE; ACETAMINOPHEN | 71179-025-28 | Vespyr Brands, Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; DOXYLAMINE SUCCINATE; ACETAMINOPHEN | 69423-807-12 | Procter & Gamble Manufacturing Company | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ASPIRIN; ACETAMINOPHEN; CAFFEINE | 21130-037-42 | BETTER LIVING BRANDS, LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 17856-7014-1 | ATLANTIC BIOLOGICALS CORP. | M | HUMAN OTC DRUG | OTC Monograph Drug |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 68210-4010-2 | SPIRIT PHARMACEUTICALS LLC | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 11822-6440-1 | Rite Aid Corporation | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE | 50066-303-04 | Genomma Lab USA | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
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