OCUFLOX (Page 3 of 3)

5 mL




solution) 0.3%

Rx Only



Carton Label
(click image for full-size original)
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
hydrochloric acid
sodium hydroxide
# 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.

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