meloxicam - 68382-051-01 - (meloxicam)

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Drug Information of meloxicam

Product NDC: 68382-051
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: 68382-051
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077921
Marketing Category: ANDA
Start Marketing Date: 20060719

Package Information of meloxicam

Package NDC: 68382-051-01
Package Description: 100 TABLET in 1 BOTTLE (68382-051-01)

NDC Information of meloxicam

NDC Code 68382-051-01
Proprietary Name meloxicam
Package Description 100 TABLET in 1 BOTTLE (68382-051-01)
Product NDC 68382-051
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name meloxicam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060719
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) 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