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Levofloxacin - 55111-281-78 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 55111-281
Proprietary Name: Levofloxacin
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 Levofloxacin

Product NDC: 55111-281
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076710
Marketing Category: ANDA
Start Marketing Date: 20110620

Package Information of Levofloxacin

Package NDC: 55111-281-78
Package Description: 10 BLISTER PACK in 1 CARTON (55111-281-78) > 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-281-79)

NDC Information of Levofloxacin

NDC Code 55111-281-78
Proprietary Name Levofloxacin
Package Description 10 BLISTER PACK in 1 CARTON (55111-281-78) > 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-281-79)
Product NDC 55111-281
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 Dr. Reddy's Laboratories Limited
Substance Name LEVOFLOXACIN
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Levofloxacin


General Information