LEVAQUIN - 67296-0372-2 - (levofloxacin)

Alphabetical Index


Drug Information of LEVAQUIN

Product NDC: 67296-0372
Proprietary Name: LEVAQUIN
Non Proprietary Name: levofloxacin
Active Ingredient(s): 500    mg/1 & nbsp;   levofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of LEVAQUIN

Product NDC: 67296-0372
Labeler Name: RedPharm Drug Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020634
Marketing Category: NDA
Start Marketing Date: 19961220

Package Information of LEVAQUIN

Package NDC: 67296-0372-2
Package Description: 7 TABLET, FILM COATED in 1 BOTTLE (67296-0372-2)

NDC Information of LEVAQUIN

NDC Code 67296-0372-2
Proprietary Name LEVAQUIN
Package Description 7 TABLET, FILM COATED in 1 BOTTLE (67296-0372-2)
Product NDC 67296-0372
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19961220
Marketing Category Name NDA
Labeler Name RedPharm Drug Inc.
Substance Name LEVOFLOXACIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of LEVAQUIN


General Information