IBU - 63739-444-01 - (Ibuprofen)

Alphabetical Index


Drug Information of IBU

Product NDC: 63739-444
Proprietary Name: IBU
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 800    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of IBU

Product NDC: 63739-444
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075682
Marketing Category: ANDA
Start Marketing Date: 20090617

Package Information of IBU

Package NDC: 63739-444-01
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-444-01) > 30 TABLET in 1 BLISTER PACK

NDC Information of IBU

NDC Code 63739-444-01
Proprietary Name IBU
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-444-01) > 30 TABLET in 1 BLISTER PACK
Product NDC 63739-444
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090617
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
Substance Name IBUPROFEN
Strength Number 800
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of IBU


General Information