Meloxicam - 49349-387-02 - (Meloxicam)

Alphabetical Index


Drug Information of Meloxicam

Product NDC: 49349-387
Proprietary Name: Meloxicam
Non Proprietary Name: Meloxicam
Active Ingredient(s): 15    mg/1 & nbsp;   Meloxicam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Meloxicam

Product NDC: 49349-387
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077927
Marketing Category: ANDA
Start Marketing Date: 20110718

Package Information of Meloxicam

Package NDC: 49349-387-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-387-02)

NDC Information of Meloxicam

NDC Code 49349-387-02
Proprietary Name Meloxicam
Package Description 30 TABLET in 1 BLISTER PACK (49349-387-02)
Product NDC 49349-387
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meloxicam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110718
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name MELOXICAM
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Meloxicam


General Information