LEVAQUIN - 21695-519-07 - (levofloxacin)

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Drug Information of LEVAQUIN

Product NDC: 21695-519
Proprietary Name: LEVAQUIN
Non Proprietary Name: levofloxacin
Active Ingredient(s): 750    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: 21695-519
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020634
Marketing Category: NDA
Start Marketing Date: 19961220

Package Information of LEVAQUIN

Package NDC: 21695-519-07
Package Description: 7 TABLET, FILM COATED in 1 BOTTLE (21695-519-07)

NDC Information of LEVAQUIN

NDC Code 21695-519-07
Proprietary Name LEVAQUIN
Package Description 7 TABLET, FILM COATED in 1 BOTTLE (21695-519-07)
Product NDC 21695-519
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 Rebel Distributors Corp
Substance Name LEVOFLOXACIN
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of LEVAQUIN


General Information