meloxicam - 68788-9898-2 - (meloxicam)

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Drug Information of meloxicam

Product NDC: 68788-9898
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: 68788-9898
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077921
Marketing Category: ANDA
Start Marketing Date: 20120214

Package Information of meloxicam

Package NDC: 68788-9898-2
Package Description: 20 TABLET in 1 BOTTLE (68788-9898-2)

NDC Information of meloxicam

NDC Code 68788-9898-2
Proprietary Name meloxicam
Package Description 20 TABLET in 1 BOTTLE (68788-9898-2)
Product NDC 68788-9898
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name meloxicam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120214
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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