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 | 21695-008-60 | Rebel Distributors Corp. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 68016-336-01 | Premier Value | ANDA076200 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 0363-0143-03 | Walgreens Co. | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
ACETAMINOPHEN | 70677-1138-2 | Strategic Sourcing Services LLC | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 59779-802-08 | CVS Pharmacy | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE | 11822-4099-0 | Rite Aid Corporation | part341 | HUMAN OTC DRUG | OTC monograph final |
IBUPROFEN; ACETAMINOPHEN | 11673-924-75 | TARGET CORPORATION | ANDA216994 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 79903-155-48 | WALMART INC. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE | 63868-764-06 | Chain Drug Marketing Association | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 21130-598-24 | Safeway, Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 59779-161-10 | CVS Pharmacy | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 17856-0985-2 | Atlantic Biologicals Corps | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
ACETAMINOPHEN | 52959-002-10 | H.J. Harkins Company, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 57243-175-15 | Salado Sales, Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE | 55910-335-34 | Dolgencorp, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
GUAIFENESIN; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE | 69423-806-12 | Procter & Gamble Manufacturing Company | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 72036-098-02 | HARRIS TEETER | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 68071-2481-5 | NuCare Pharmaceuticals,Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
WATER; NEOMYCIN SULFATE; LIDOCAINE; ISOPROPYL ALCOHOL; BENZALKONIUM CHLORIDE; BENZOCAINE; IBUPROFEN; POLYMYXIN B SULFATE; ASPIRIN; ALCOHOL; ACETAMINOPHEN; BACITRACIN ZINC | 52124-0112-1 | Genuine First Aid LLC | part333 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; ACETAMINOPHEN | 41163-459-40 | United Natural Foods, Inc. dba UNFI | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 69377-002-01 | Gelpharma S.A. de C.V. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 82706-008-02 | VIVUNT PHARMA LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 41520-800-28 | American Sales Company | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; GUAIFENESIN | 36800-575-02 | TopCo Associates LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DIPHENHYDRAMINE HYDROCHLORIDE | 0067-8137-20 | Haleon US Holdings LLC | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 17856-0045-8 | ATLANTIC BIOLOGICALS CORP. | M | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 69618-011-01 | Reliable 1 Laboratories LLC | part343 | HUMAN OTC DRUG | OTC monograph not final |
PHENYLEPHRINE HYDROCHLORIDE; CHLORPHENIRAMINE MALEATE; ACETAMINOPHEN | 63029-221-12 | Medtech Products Inc. | part341 | HUMAN OTC DRUG | OTC MONOGRAPH FINAL |
ACETAMINOPHEN | 0363-0590-16 | Walgreen Company | part343 | HUMAN OTC DRUG | OTC monograph not final |
ASPIRIN; CAFFEINE; ACETAMINOPHEN | 59779-374-87 | CVS Pharmacy | ANDA075794 | HUMAN OTC DRUG | ANDA |
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