Meloxicam - 21695-076-90 - (Meloxicam)

Alphabetical Index


Drug Information of Meloxicam

Product NDC: 21695-076
Proprietary Name: Meloxicam
Non Proprietary Name: Meloxicam
Active Ingredient(s): 7.5    mg/1 & nbsp;   Meloxicam
Administration Route(s):
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Meloxicam

Product NDC: 21695-076
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077927
Marketing Category: ANDA
Start Marketing Date: 20061220

Package Information of Meloxicam

Package NDC: 21695-076-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (21695-076-90)

NDC Information of Meloxicam

NDC Code 21695-076-90
Proprietary Name Meloxicam
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (21695-076-90)
Product NDC 21695-076
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meloxicam
Dosage Form Name TABLET
Route Name
Start Marketing Date 20061220
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
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