Ibuprofen - 37205-670-90 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 37205-670
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: 37205-670
Labeler Name: CARDINAL HEALTH
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075010
Marketing Category: ANDA
Start Marketing Date: 19880524

Package Information of Ibuprofen

Package NDC: 37205-670-90
Package Description: 1 BOTTLE in 1 CARTON (37205-670-90) > 500 TABLET in 1 BOTTLE

NDC Information of Ibuprofen

NDC Code 37205-670-90
Proprietary Name Ibuprofen
Package Description 1 BOTTLE in 1 CARTON (37205-670-90) > 500 TABLET in 1 BOTTLE
Product NDC 37205-670
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 CARDINAL HEALTH
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information