meloxicam - 55289-272-20 - (meloxicam)

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Drug Information of meloxicam

Product NDC: 55289-272
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: 55289-272
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077927
Marketing Category: ANDA
Start Marketing Date: 20070307

Package Information of meloxicam

Package NDC: 55289-272-20
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (55289-272-20)

NDC Information of meloxicam

NDC Code 55289-272-20
Proprietary Name meloxicam
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (55289-272-20)
Product NDC 55289-272
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name meloxicam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070307
Marketing Category Name ANDA
Labeler Name PD-Rx 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