CELEBREX - 49349-872-20 - (CELECOXIB)

Alphabetical Index


Drug Information of CELEBREX

Product NDC: 49349-872
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: 49349-872
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020998
Marketing Category: NDA
Start Marketing Date: 20130220

Package Information of CELEBREX

Package NDC: 49349-872-20
Package Description: 100 CAPSULE in 1 VIAL (49349-872-20)

NDC Information of CELEBREX

NDC Code 49349-872-20
Proprietary Name CELEBREX
Package Description 100 CAPSULE in 1 VIAL (49349-872-20)
Product NDC 49349-872
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CELECOXIB
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130220
Marketing Category Name NDA
Labeler Name REMEDYREPACK 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