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Pain Relief PM - 41163-214-50 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of Pain Relief PM

Product NDC: 41163-214
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
Coding System: National Drug Codes(NDC)

Labeler Information of Pain Relief PM

Product NDC: 41163-214
Labeler Name: SuperValu (Equaline)
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130325

Package Information of Pain Relief PM

Package NDC: 41163-214-50
Package Description: 1 BOTTLE in 1 BOX (41163-214-50) > 50 TABLET in 1 BOTTLE

NDC Information of Pain Relief PM

NDC Code 41163-214-50
Proprietary Name Pain Relief PM
Package Description 1 BOTTLE in 1 BOX (41163-214-50) > 50 TABLET in 1 BOTTLE
Product NDC 41163-214
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130325
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name SuperValu (Equaline)
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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