OCUFLOX (Page 3 of 3)

5 mL

Ocuflox®

(ofloxacin

ophthalmic

solution) 0.3%

Rx Only

STERILE

ALLERGAN

Carton Label
(click image for full-size original)
OCUFLOX
ofloxacin solution/ drops
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:11980-779
Route of Administration OPHTHALMIC DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ofloxacin (ofloxacin) ofloxacin 3 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
benzalkonium chloride
sodium chloride
water
hydrochloric acid
sodium hydroxide
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:11980-779-05 1 BOTTLE, DROPPER in 1 CARTON contains a BOTTLE, DROPPER
1 5 mL in 1 BOTTLE, DROPPER This package is contained within the CARTON (11980-779-05)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA019921 08/01/1993
Labeler — Allergan, Inc. (144796497)

Revised: 04/2017 Allergan, Inc.

Page 3 of 3 1 2 3

All MedLibrary.org resources are included in as near-original form as possible, meaning that the information from the original provider has been rendered here with only typographical or stylistic modifications and not with any substantive alterations of content, meaning or intent.

This site is provided for educational and informational purposes only, in accordance with our Terms of Use, and is not intended as a substitute for the advice of a medical doctor, nurse, nurse practitioner or other qualified health professional.

Privacy Policy | Copyright © 2023. All Rights Reserved.