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Levofloxacin - 68180-240-13 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 68180-240
Proprietary Name: Levofloxacin
Non Proprietary Name: Levofloxacin
Active Ingredient(s): 250    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: 68180-240
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078424
Marketing Category: ANDA
Start Marketing Date: 20110620

Package Information of Levofloxacin

Package NDC: 68180-240-13
Package Description: 10 BLISTER PACK in 1 CARTON (68180-240-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68180-240-11)

NDC Information of Levofloxacin

NDC Code 68180-240-13
Proprietary Name Levofloxacin
Package Description 10 BLISTER PACK in 1 CARTON (68180-240-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68180-240-11)
Product NDC 68180-240
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 Lupin Pharmaceuticals, Inc.
Substance Name LEVOFLOXACIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Levofloxacin


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