CELEBREX - 54569-4672-1 - (Celecoxib)

Alphabetical Index


Drug Information of CELEBREX

Product NDC: 54569-4672
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: 54569-4672
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020998
Marketing Category: NDA
Start Marketing Date: 19990125

Package Information of CELEBREX

Package NDC: 54569-4672-1
Package Description: 14 CAPSULE in 1 BOTTLE (54569-4672-1)

NDC Information of CELEBREX

NDC Code 54569-4672-1
Proprietary Name CELEBREX
Package Description 14 CAPSULE in 1 BOTTLE (54569-4672-1)
Product NDC 54569-4672
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Celecoxib
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19990125
Marketing Category Name NDA
Labeler Name A-S Medication Solutions LLC
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