CELEBREX - 52959-540-21 - (Celecoxib)

Alphabetical Index


Drug Information of CELEBREX

Product NDC: 52959-540
Proprietary Name: CELEBREX
Non Proprietary Name: Celecoxib
Active Ingredient(s): 100    mg/1 & nbsp;   Celecoxib
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of CELEBREX

Product NDC: 52959-540
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020998
Marketing Category: NDA
Start Marketing Date: 19981002

Package Information of CELEBREX

Package NDC: 52959-540-21
Package Description: 21 CAPSULE in 1 BOTTLE (52959-540-21)

NDC Information of CELEBREX

NDC Code 52959-540-21
Proprietary Name CELEBREX
Package Description 21 CAPSULE in 1 BOTTLE (52959-540-21)
Product NDC 52959-540
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 H.J. Harkins Company, Inc.
Substance Name CELECOXIB
Strength Number 100
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