Ibuprofen - 67046-303-30 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 67046-303
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: 67046-303
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA072096
Marketing Category: ANDA
Start Marketing Date: 20100802

Package Information of Ibuprofen

Package NDC: 67046-303-30
Package Description: 30 TABLET in 1 BLISTER PACK (67046-303-30)

NDC Information of Ibuprofen

NDC Code 67046-303-30
Proprietary Name Ibuprofen
Package Description 30 TABLET in 1 BLISTER PACK (67046-303-30)
Product NDC 67046-303
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100802
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information