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Levofloxacin - 21695-027-03 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 21695-027
Proprietary Name: Levofloxacin
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 Levofloxacin

Product NDC: 21695-027
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076361
Marketing Category: ANDA
Start Marketing Date: 20110620

Package Information of Levofloxacin

Package NDC: 21695-027-03
Package Description: 3 TABLET, FILM COATED in 1 BOTTLE (21695-027-03)

NDC Information of Levofloxacin

NDC Code 21695-027-03
Proprietary Name Levofloxacin
Package Description 3 TABLET, FILM COATED in 1 BOTTLE (21695-027-03)
Product NDC 21695-027
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110620
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name LEVOFLOXACIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Levofloxacin


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