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Pain Relief PM - 59779-556-76 - (Acetaminophen, Diphenhydramin HCl)

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Drug Information of Pain Relief PM

Product NDC: 59779-556
Proprietary Name: Pain Relief PM
Non Proprietary Name: Acetaminophen, Diphenhydramin HCl
Active Ingredient(s): 500; 25    mg/1; mg/1 & nbsp;   Acetaminophen, Diphenhydramin HCl
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Pain Relief PM

Product NDC: 59779-556
Labeler Name: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20071217

Package Information of Pain Relief PM

Package NDC: 59779-556-76
Package Description: 450 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (59779-556-76)

NDC Information of Pain Relief PM

NDC Code 59779-556-76
Proprietary Name Pain Relief PM
Package Description 450 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (59779-556-76)
Product NDC 59779-556
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramin HCl
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20071217
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
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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