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Extra Strength Pain Reliever PM - 70253-556-10 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of Extra Strength Pain Reliever PM

Product NDC: 70253-556
Proprietary Name: Extra Strength 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): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Extra Strength Pain Reliever PM

Product NDC: 70253-556
Labeler Name: NASH-FINCH COMPANY
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20071217

Package Information of Extra Strength Pain Reliever PM

Package NDC: 70253-556-10
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (70253-556-10) > 40 CAPSULE in 1 BOTTLE, PLASTIC

NDC Information of Extra Strength Pain Reliever PM

NDC Code 70253-556-10
Proprietary Name Extra Strength Pain Reliever PM
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (70253-556-10) > 40 CAPSULE in 1 BOTTLE, PLASTIC
Product NDC 70253-556
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20071217
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name NASH-FINCH COMPANY
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Extra Strength Pain Reliever PM


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