CELEBREX - 55289-475-28 - (Celecoxib)

Alphabetical Index


Drug Information of CELEBREX

Product NDC: 55289-475
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: 55289-475
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020998
Marketing Category: NDA
Start Marketing Date: 19981002

Package Information of CELEBREX

Package NDC: 55289-475-28
Package Description: 28 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55289-475-28) > 20 CAPSULE in 1 BOTTLE, PLASTIC (55289-475-20)

NDC Information of CELEBREX

NDC Code 55289-475-28
Proprietary Name CELEBREX
Package Description 28 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55289-475-28) > 20 CAPSULE in 1 BOTTLE, PLASTIC (55289-475-20)
Product NDC 55289-475
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 PD-Rx Pharmaceuticals, Inc.
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