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 | 11673-759-28 | Target Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 11673-105-28 | Target Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 11673-342-26 | TARGET CORPORATION | part343 | HUMAN OTC DRUG | OTC monograph not final |
CAFFEINE; ACETAMINOPHEN; ASPIRIN | 11673-070-01 | TARGET CORPORATION | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 11673-484-52 | Target Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; CAFFEINE; ASPIRIN | 11673-686-80 | TARGET Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DIPHENHYDRAMINE HYDROCHLORIDE; GUAIFENESIN | 11673-837-81 | Target Corporation | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 11673-241-24 | Target Corporation | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 51672-2115-0 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 51672-2114-0 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 51672-2116-0 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 51672-2115-4 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 51672-2116-4 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 51672-2114-2 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 51672-2117-0 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 51672-2115-2 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 51672-2117-4 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 51672-2116-2 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 51672-2114-4 | Taro Pharmaceuticals U.S.A. Inc. | NDA018337 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN | 51672-5320-8 | TARO PHARMACEUTICALS U.S.A., INC. | part343 | HUMAN OTC DRUG | OTC monograph not final |
CAFFEINE; ACETAMINOPHEN; BUTALBITAL | 51672-4222-1 | Taro Pharmaceuticals U.S.A., Inc. | ANDA213046 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 51672-5319-8 | TARO PHARMACEUTICALS U.S.A., INC. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 42912-0153-6 | TDS Pharm., Co., Ltd. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 42912-0152-7 | TDS Pharm., Co., Ltd. | part343 | HUMAN OTC DRUG | OTC monograph not final |
DIPHENHYDRAMINE HYDROCHLORIDE; ACETAMINOPHEN | 42912-0154-2 | TDS Pharm., Co., Ltd. | part343 | HUMAN OTC DRUG | OTC monograph not final |
LIDOCAINE HYDROCHLORIDE; ACETAMINOPHEN; BENZALKONIUM CHLORIDE; ASPIRIN; AMMONIA; IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE | 44224-2999-0 | Tender Corporation | part333A | HUMAN OTC DRUG | OTC monograph not final |
ALCOHOL; ACETAMINOPHEN; POLYMYXIN B SULFATE; BENZALKONIUM CHLORIDE; BENZOCAINE; IBUPROFEN; NEOMYCIN SULFATE; BACITRACIN ZINC | 44224-0699-5 | Tender Corporation DBA Adventure Ready Brands | part348 | HUMAN OTC DRUG | OTC monograph final |
NEOMYCIN SULFATE; BENZALKONIUM CHLORIDE; IBUPROFEN; ALCOHOL; ACETAMINOPHEN; BACITRACIN ZINC; POLYMYXIN B SULFATE; BENZOCAINE | 44224-0999-5 | Tender Corporation DBA Adventure Ready Brands | part348 | HUMAN OTC DRUG | OTC monograph final |
ASPIRIN; BENZALKONIUM CHLORIDE; DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN; BENZOCAINE; NEOMYCIN SULFATE; ALCOHOL; BACITRACIN ZINC; POLYMYXIN B SULFATE; ACETAMINOPHEN | 44224-2000-1 | Tender Corporation DBA Adventure Ready Brands | part333B | HUMAN OTC DRUG | OTC monograph not final |
DIPHENHYDRAMINE HYDROCHLORIDE; BENZALKONIUM CHLORIDE; NEOMYCIN SULFATE; ASPIRIN; POVIDONE-IODINE; IBUPROFEN; ACETAMINOPHEN; POLYMYXIN B SULFATE; BACITRACIN ZINC | 44224-0118-1 | Tender Corporation DBA Adventure Ready Brands | part333A | HUMAN OTC DRUG | OTC monograph final |
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