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

Extra Strength Pain Reliever - 70253-519-15 - (Acetaminophen)

Alphabetical Index


Drug Information of Extra Strength Pain Reliever

Product NDC: 70253-519
Proprietary Name: Extra Strength Pain Reliever
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Extra Strength Pain Reliever

Product NDC: 70253-519
Labeler Name: NASH-FINCH COMPANY
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20040510

Package Information of Extra Strength Pain Reliever

Package NDC: 70253-519-15
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (70253-519-15) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC

NDC Information of Extra Strength Pain Reliever

NDC Code 70253-519-15
Proprietary Name Extra Strength Pain Reliever
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (70253-519-15) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
Product NDC 70253-519
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20040510
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name NASH-FINCH COMPANY
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Extra Strength Pain Reliever


General Information