Meloxicam - 10544-252-30 - (Meloxicam)

Alphabetical Index


Drug Information of Meloxicam

Product NDC: 10544-252
Proprietary Name: Meloxicam
Non Proprietary Name: Meloxicam
Active Ingredient(s): 7.5    mg/1 & nbsp;   Meloxicam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Meloxicam

Product NDC: 10544-252
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077944
Marketing Category: ANDA
Start Marketing Date: 20100413

Package Information of Meloxicam

Package NDC: 10544-252-30
Package Description: 30 TABLET in 1 BOTTLE (10544-252-30)

NDC Information of Meloxicam

NDC Code 10544-252-30
Proprietary Name Meloxicam
Package Description 30 TABLET in 1 BOTTLE (10544-252-30)
Product NDC 10544-252
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meloxicam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100413
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, Inc.
Substance Name MELOXICAM
Strength Number 7.5
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