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Pain Reliever PM - 0363-0213-50 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of Pain Reliever PM

Product NDC: 0363-0213
Proprietary Name: 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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Pain Reliever PM

Product NDC: 0363-0213
Labeler Name: Walgreens
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130531

Package Information of Pain Reliever PM

Package NDC: 0363-0213-50
Package Description: 1 BOTTLE, PLASTIC in 1 BOX (0363-0213-50) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Information of Pain Reliever PM

NDC Code 0363-0213-50
Proprietary Name Pain Reliever PM
Package Description 1 BOTTLE, PLASTIC in 1 BOX (0363-0213-50) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC
Product NDC 0363-0213
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20130531
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Walgreens
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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