LEVAQUIN - 54868-3923-7 - (levofloxacin)

Alphabetical Index


Drug Information of LEVAQUIN

Product NDC: 54868-3923
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: 54868-3923
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020634
Marketing Category: NDA
Start Marketing Date: 20000511

Package Information of LEVAQUIN

Package NDC: 54868-3923-7
Package Description: 14 TABLET, FILM COATED in 1 BOTTLE (54868-3923-7)

NDC Information of LEVAQUIN

NDC Code 54868-3923-7
Proprietary Name LEVAQUIN
Package Description 14 TABLET, FILM COATED in 1 BOTTLE (54868-3923-7)
Product NDC 54868-3923
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20000511
Marketing Category Name NDA
Labeler Name Physicians Total Care, 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