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levofloxacin - 68788-9695-2 - (levofloxacin)

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Drug Information of levofloxacin

Product NDC: 68788-9695
Proprietary Name: levofloxacin
Non Proprietary Name: levofloxacin
Active Ingredient(s): 750    mg/1 & nbsp;   levofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of levofloxacin

Product NDC: 68788-9695
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090722
Marketing Category: ANDA
Start Marketing Date: 20130327

Package Information of levofloxacin

Package NDC: 68788-9695-2
Package Description: 20 TABLET in 1 BOTTLE (68788-9695-2)

NDC Information of levofloxacin

NDC Code 68788-9695-2
Proprietary Name levofloxacin
Package Description 20 TABLET in 1 BOTTLE (68788-9695-2)
Product NDC 68788-9695
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levofloxacin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130327
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
Substance Name LEVOFLOXACIN
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of levofloxacin


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