Meloxicam - 61442-127-10 - (Meloxicam)

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Drug Information of Meloxicam

Product NDC: 61442-127
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: 61442-127
Labeler Name: Carlsbad Technology, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077918
Marketing Category: ANDA
Start Marketing Date: 20091201

Package Information of Meloxicam

Package NDC: 61442-127-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (61442-127-10)

NDC Information of Meloxicam

NDC Code 61442-127-10
Proprietary Name Meloxicam
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (61442-127-10)
Product NDC 61442-127
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meloxicam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091201
Marketing Category Name ANDA
Labeler Name Carlsbad Technology, 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