LEVAQUIN - 10147-0941-6 - (levofloxacin)

Alphabetical Index


Drug Information of LEVAQUIN

Product NDC: 10147-0941
Proprietary Name: LEVAQUIN
Non Proprietary Name: levofloxacin
Active Ingredient(s): 25    mg/mL & nbsp;   levofloxacin
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of LEVAQUIN

Product NDC: 10147-0941
Labeler Name: Patriot Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021721
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20130701

Package Information of LEVAQUIN

Package NDC: 10147-0941-6
Package Description: 1 BOTTLE in 1 CARTON (10147-0941-6) > 480 mL in 1 BOTTLE

NDC Information of LEVAQUIN

NDC Code 10147-0941-6
Proprietary Name LEVAQUIN
Package Description 1 BOTTLE in 1 CARTON (10147-0941-6) > 480 mL in 1 BOTTLE
Product NDC 10147-0941
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levofloxacin
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20130701
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Patriot Pharmaceuticals, Inc.
Substance Name LEVOFLOXACIN
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of LEVAQUIN


General Information