Ibuprofen - 63981-291-14 - (ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 63981-291
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: 63981-291
Labeler Name: COSTCO WHOLESALE CORPORATION
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075010
Marketing Category: ANDA
Start Marketing Date: 19990302

Package Information of Ibuprofen

Package NDC: 63981-291-14
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63981-291-14)

NDC Information of Ibuprofen

NDC Code 63981-291-14
Proprietary Name Ibuprofen
Package Description 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63981-291-14)
Product NDC 63981-291
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19990302
Marketing Category Name ANDA
Labeler Name COSTCO WHOLESALE CORPORATION
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information