Ibuprofen - 70253-392-15 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 70253-392
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 70253-392
Labeler Name: NASH-FINCH COMPANY
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075139
Marketing Category: ANDA
Start Marketing Date: 20020330

Package Information of Ibuprofen

Package NDC: 70253-392-15
Package Description: 1 BOTTLE in 1 CARTON (70253-392-15) > 50 TABLET, FILM COATED in 1 BOTTLE

NDC Information of Ibuprofen

NDC Code 70253-392-15
Proprietary Name Ibuprofen
Package Description 1 BOTTLE in 1 CARTON (70253-392-15) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC 70253-392
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20020330
Marketing Category Name ANDA
Labeler Name NASH-FINCH COMPANY
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information