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Pain reliever PM - 49348-918-09 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of Pain reliever PM

Product NDC: 49348-918
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
Coding System: National Drug Codes(NDC)

Labeler Information of Pain reliever PM

Product NDC: 49348-918
Labeler Name: Mckesson (Sunmark)
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110524

Package Information of Pain reliever PM

Package NDC: 49348-918-09
Package Description: 1 BOTTLE in 1 CARTON (49348-918-09) > 50 TABLET in 1 BOTTLE

NDC Information of Pain reliever PM

NDC Code 49348-918-09
Proprietary Name Pain reliever PM
Package Description 1 BOTTLE in 1 CARTON (49348-918-09) > 50 TABLET in 1 BOTTLE
Product NDC 49348-918
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110524
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Mckesson (Sunmark)
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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