CELEBREX - 55154-3622-0 - (Celecoxib)

Alphabetical Index


Drug Information of CELEBREX

Product NDC: 55154-3622
Proprietary Name: CELEBREX
Non Proprietary Name: Celecoxib
Active Ingredient(s): 200    mg/1 & nbsp;   Celecoxib
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of CELEBREX

Product NDC: 55154-3622
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020998
Marketing Category: NDA
Start Marketing Date: 19981002

Package Information of CELEBREX

Package NDC: 55154-3622-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-3622-0) > 1 CAPSULE in 1 BLISTER PACK

NDC Information of CELEBREX

NDC Code 55154-3622-0
Proprietary Name CELEBREX
Package Description 10 BLISTER PACK in 1 BAG (55154-3622-0) > 1 CAPSULE in 1 BLISTER PACK
Product NDC 55154-3622
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Celecoxib
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19981002
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name CELECOXIB
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of CELEBREX


General Information