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equaline pain relief pm - 41163-437-71 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of equaline pain relief pm

Product NDC: 41163-437
Proprietary Name: equaline pain relief 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 equaline pain relief pm

Product NDC: 41163-437
Labeler Name: Supervalu Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20040830

Package Information of equaline pain relief pm

Package NDC: 41163-437-71
Package Description: 1 BOTTLE in 1 CARTON (41163-437-71) > 50 TABLET, FILM COATED in 1 BOTTLE

NDC Information of equaline pain relief pm

NDC Code 41163-437-71
Proprietary Name equaline pain relief pm
Package Description 1 BOTTLE in 1 CARTON (41163-437-71) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC 41163-437
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040830
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Supervalu Inc
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of equaline pain relief pm


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