Meloxicam - 66116-439-30 - (Meloxicam)

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Drug Information of Meloxicam

Product NDC: 66116-439
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: 66116-439
Labeler Name: MedVantx, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077936
Marketing Category: ANDA
Start Marketing Date: 20101014

Package Information of Meloxicam

Package NDC: 66116-439-30
Package Description: 30 TABLET in 1 BOTTLE (66116-439-30)

NDC Information of Meloxicam

NDC Code 66116-439-30
Proprietary Name Meloxicam
Package Description 30 TABLET in 1 BOTTLE (66116-439-30)
Product NDC 66116-439
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meloxicam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101014
Marketing Category Name ANDA
Labeler Name MedVantx, 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