Mobic - 0597-0029-01 - (meloxicam)

Alphabetical Index


Drug Information of Mobic

Product NDC: 0597-0029
Proprietary Name: Mobic
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 Mobic

Product NDC: 0597-0029
Labeler Name: Boehringer Ingelheim Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020938
Marketing Category: NDA
Start Marketing Date: 20000601

Package Information of Mobic

Package NDC: 0597-0029-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0597-0029-01)

NDC Information of Mobic

NDC Code 0597-0029-01
Proprietary Name Mobic
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0597-0029-01)
Product NDC 0597-0029
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name meloxicam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000601
Marketing Category Name NDA
Labeler Name Boehringer Ingelheim 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 Mobic


General Information