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sunmark pain reliever pm - 49348-349-09 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of sunmark pain reliever pm

Product NDC: 49348-349
Proprietary Name: sunmark pain reliever pm
Non Proprietary Name: Acetaminophen, Diphenhydramine HCl
Active Ingredient(s): 500; 25    mg/1; mg/1 & nbsp;   Acetaminophen, Diphenhydramine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of sunmark pain reliever pm

Product NDC: 49348-349
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20030811

Package Information of sunmark pain reliever pm

Package NDC: 49348-349-09
Package Description: 1 BOTTLE in 1 CARTON (49348-349-09) > 50 TABLET, FILM COATED in 1 BOTTLE

NDC Information of sunmark pain reliever pm

NDC Code 49348-349-09
Proprietary Name sunmark pain reliever pm
Package Description 1 BOTTLE in 1 CARTON (49348-349-09) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC 49348-349
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030811
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of sunmark pain reliever pm


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