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ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE - 65437-041-31 - (ACETAMINOPHEN and DIPHENHYDRAMINE HYDROCHLORIDE)

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Drug Information of ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE

Product NDC: 65437-041
Proprietary Name: ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE
Non Proprietary Name: ACETAMINOPHEN and DIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient(s): 500; 25    mg/1; mg/1 & nbsp;   ACETAMINOPHEN and DIPHENHYDRAMINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE

Product NDC: 65437-041
Labeler Name: HIMPRIT PHARMACHEM PVT LTD
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100701

Package Information of ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE

Package NDC: 65437-041-31
Package Description: 1 BAG in 1 DRUM (65437-041-31) > 31000 TABLET, FILM COATED in 1 BAG

NDC Information of ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE

NDC Code 65437-041-31
Proprietary Name ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE
Package Description 1 BAG in 1 DRUM (65437-041-31) > 31000 TABLET, FILM COATED in 1 BAG
Product NDC 65437-041
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACETAMINOPHEN and DIPHENHYDRAMINE HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100701
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name HIMPRIT PHARMACHEM PVT LTD
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE


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