Ibuprofen - 70253-291-12 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 70253-291
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 70253-291
Labeler Name: NASH-FINCH COMPANY
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075010
Marketing Category: ANDA
Start Marketing Date: 19880524

Package Information of Ibuprofen

Package NDC: 70253-291-12
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (70253-291-12) > 100 TABLET in 1 BOTTLE, PLASTIC

NDC Information of Ibuprofen

NDC Code 70253-291-12
Proprietary Name Ibuprofen
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (70253-291-12) > 100 TABLET in 1 BOTTLE, PLASTIC
Product NDC 70253-291
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880524
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