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Pain Reliever PM - 70253-235-08 - (Acetaminophen and Diphenhydramine HCl)

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Drug Information of Pain Reliever PM

Product NDC: 70253-235
Proprietary Name: Pain Reliever PM
Non Proprietary Name: Acetaminophen and Diphenhydramine HCl
Active Ingredient(s): 500; 25    mg/1; mg/1 & nbsp;   Acetaminophen and Diphenhydramine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Pain Reliever PM

Product NDC: 70253-235
Labeler Name: NASH-FINCH COMPANY
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19940515

Package Information of Pain Reliever PM

Package NDC: 70253-235-08
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (70253-235-08) > 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of Pain Reliever PM

NDC Code 70253-235-08
Proprietary Name Pain Reliever PM
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (70253-235-08) > 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 70253-235
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and Diphenhydramine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19940515
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name NASH-FINCH COMPANY
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Pain Reliever PM


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