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Pain Relief PM - 41163-229-50 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of Pain Relief PM

Product NDC: 41163-229
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: 41163-229
Labeler Name: EQUALINE (SuperValu)
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120919

Package Information of Pain Relief PM

Package NDC: 41163-229-50
Package Description: 1 BOTTLE, PLASTIC in 1 BOX (41163-229-50) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Information of Pain Relief PM

NDC Code 41163-229-50
Proprietary Name Pain Relief PM
Package Description 1 BOTTLE, PLASTIC in 1 BOX (41163-229-50) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC
Product NDC 41163-229
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20120919
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name EQUALINE (SuperValu)
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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