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Extra Strength Pain Relief PM - 59779-235-13 - (Acetaminophen and Diphenhydramine HCl)

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Drug Information of Extra Strength Pain Relief PM

Product NDC: 59779-235
Proprietary Name: Extra Strength Pain Relief 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 Extra Strength Pain Relief PM

Product NDC: 59779-235
Labeler Name: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19940515

Package Information of Extra Strength Pain Relief PM

Package NDC: 59779-235-13
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (59779-235-13) > 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of Extra Strength Pain Relief PM

NDC Code 59779-235-13
Proprietary Name Extra Strength Pain Relief PM
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (59779-235-13) > 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 59779-235
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 WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Extra Strength Pain Relief PM


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