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Pain Relief PM - 36800-361-50 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of Pain Relief PM

Product NDC: 36800-361
Proprietary Name: 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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Pain Relief PM

Product NDC: 36800-361
Labeler Name: Topco Associates LLC (Top Care)
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121019

Package Information of Pain Relief PM

Package NDC: 36800-361-50
Package Description: 1 BOTTLE in 1 CARTON (36800-361-50) > 50 TABLET, COATED in 1 BOTTLE

NDC Information of Pain Relief PM

NDC Code 36800-361-50
Proprietary Name Pain Relief PM
Package Description 1 BOTTLE in 1 CARTON (36800-361-50) > 50 TABLET, COATED in 1 BOTTLE
Product NDC 36800-361
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20121019
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Topco Associates LLC (Top Care)
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Pain Relief PM


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