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Acetaminophen, Diphenhydramine Hydrochloride - 57344-101-05 - (ACETAMINOPHEN and DIPHENHYDRAMINE HYDROCHLORIDE)

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Drug Information of Acetaminophen, Diphenhydramine Hydrochloride

Product NDC: 57344-101
Proprietary Name: Acetaminophen, Diphenhydramine Hydrochloride
Non Proprietary Name: ACETAMINOPHEN and DIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient(s): 500; 12.5    mg/1; mg/1 & nbsp;   ACETAMINOPHEN and DIPHENHYDRAMINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen, Diphenhydramine Hydrochloride

Product NDC: 57344-101
Labeler Name: AAA Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121222

Package Information of Acetaminophen, Diphenhydramine Hydrochloride

Package NDC: 57344-101-05
Package Description: 4 BLISTER PACK in 1 CARTON (57344-101-05) > 12 TABLET, COATED in 1 BLISTER PACK

NDC Information of Acetaminophen, Diphenhydramine Hydrochloride

NDC Code 57344-101-05
Proprietary Name Acetaminophen, Diphenhydramine Hydrochloride
Package Description 4 BLISTER PACK in 1 CARTON (57344-101-05) > 12 TABLET, COATED in 1 BLISTER PACK
Product NDC 57344-101
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACETAMINOPHEN and DIPHENHYDRAMINE HYDROCHLORIDE
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20121222
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name AAA Pharmaceutical, Inc.
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 12.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen, Diphenhydramine Hydrochloride


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