ZYMAXID - 0023-3615-01 - (gatifloxacin)

Alphabetical Index


Drug Information of ZYMAXID

Product NDC: 0023-3615
Proprietary Name: ZYMAXID
Non Proprietary Name: gatifloxacin
Active Ingredient(s): 5    mg/mL & nbsp;   gatifloxacin
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of ZYMAXID

Product NDC: 0023-3615
Labeler Name: Allergan, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022548
Marketing Category: NDA
Start Marketing Date: 20100519

Package Information of ZYMAXID

Package NDC: 0023-3615-01
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (0023-3615-01) > 1 mL in 1 BOTTLE, DROPPER

NDC Information of ZYMAXID

NDC Code 0023-3615-01
Proprietary Name ZYMAXID
Package Description 1 BOTTLE, DROPPER in 1 CARTON (0023-3615-01) > 1 mL in 1 BOTTLE, DROPPER
Product NDC 0023-3615
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name gatifloxacin
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20100519
Marketing Category Name NDA
Labeler Name Allergan, Inc.
Substance Name GATIFLOXACIN
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of ZYMAXID


General Information