Home > National Drug Code (NDC) > Extra Strength Pain Relief

Extra Strength Pain Relief - 59779-751-15 - (Acetaminophen)

Alphabetical Index


Drug Information of Extra Strength Pain Relief

Product NDC: 59779-751
Proprietary Name: Extra Strength Pain Relief
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Extra Strength Pain Relief

Product NDC: 59779-751
Labeler Name: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19930402

Package Information of Extra Strength Pain Relief

Package NDC: 59779-751-15
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (59779-751-15) > 50 TABLET in 1 BOTTLE, PLASTIC

NDC Information of Extra Strength Pain Relief

NDC Code 59779-751-15
Proprietary Name Extra Strength Pain Relief
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (59779-751-15) > 50 TABLET in 1 BOTTLE, PLASTIC
Product NDC 59779-751
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930402
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Extra Strength Pain Relief


General Information