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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CAFFEINE; ACETAMINOPHEN; ASPIRIN | 21130-959-08 | Better Living Brands, LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 63941-288-04 | Best Choice (Valu Merchandisers Company) | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; IBUPROFEN | 0573-0147-09 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; ACETAMINOPHEN | 76168-119-25 | Velocity Pharma | part343 | HUMAN OTC DRUG | OTC monograph not final |
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN | 11822-1583-1 | Rite Aid Corporation | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 67091-213-24 | WinCo Foods, LLC | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 47682-173-50 | Unifirst First Aid Corporation | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 63868-084-20 | Chain Drug Marketing Association | part343 | HUMAN OTC DRUG | OTC monograph not final |
DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; ACETAMINOPHEN | 11673-757-83 | TARGET CORPORATION | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 55910-691-10 | Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 56062-590-16 | Publix Super Markets Inc | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 68016-336-50 | Premier Value | ANDA076200 | HUMAN OTC DRUG | ANDA |
DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 59726-050-24 | P & L Development, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68016-141-04 | Chain Drug Consortium (Premier Value) | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
ACETAMINOPHEN | 21130-431-01 | BETTER LIVING BRANDS LLC. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 11822-2350-7 | Rite Aid Corporation | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE | 50580-507-04 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN | 68163-749-08 | RARITAN PHARMACEUTICALS | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 49483-693-48 | TIME CAP LABORATORIES, INC. | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 0067-6094-01 | Haleon US Holdings LLC | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 51672-2115-2 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 41250-484-76 | Meijer Distribution Inc | part343 | HUMAN OTC DRUG | OTC monograph not final |
PYRILAMINE MALEATE; CAFFEINE; ACETAMINOPHEN | 0280-8005-16 | Bayer HealthCare LLC. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE | 36800-474-02 | TOPCO ASSOCIATES LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 59779-350-01 | CVS Pharmacy | ANDA076200 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 58602-760-73 | Aurohealth LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 41163-214-10 | SuperValu (Equaline) | part338 | HUMAN OTC DRUG | OTC MONOGRAPH FINAL |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 55758-010-18 | Pharmadel LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN | 59726-201-48 | P & L Development, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; IBUPROFEN | 0573-0147-90 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
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