Meloxicam - 76237-202-30 - (Meloxicam)

Alphabetical Index


Drug Information of Meloxicam

Product NDC: 76237-202
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: 76237-202
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077936
Marketing Category: ANDA
Start Marketing Date: 20111223

Package Information of Meloxicam

Package NDC: 76237-202-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-202-30) > 5 TABLET in 1 BLISTER PACK

NDC Information of Meloxicam

NDC Code 76237-202-30
Proprietary Name Meloxicam
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-202-30) > 5 TABLET in 1 BLISTER PACK
Product NDC 76237-202
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meloxicam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111223
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
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