Flurbiprofen Sodium (Page 2 of 2)

Storage:

Store at 15°–25°C (59°–77°F).

Bausch + Lomb, a division of Valeant Pharmaceuticals North America LLC
Bridgewater, NJ 08807 USA
©Bausch & Lomb Incorporated

Revised: July 2016

9100604 (Folded)

9100704 (Flat)

Principal Display Panel

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(click image for full-size original)

NDC 24208-314-25

Flurbiprofen
Sodium
Ophthalmic
Solution, USP
0.03%
(Sterile)

FOR OPHTHALMIC USE ONLY

Rx only

2.5 mL

BAUSCH + LOMB

FLURBIPROFEN SODIUM
flurbiprofen sodium solution/ drops
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:24208-314
Route of Administration OPHTHALMIC DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FLURBIPROFEN SODIUM (FLURBIPROFEN) FLURBIPROFEN SODIUM 0.3 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
CITRIC ACID MONOHYDRATE
EDETATE DISODIUM
HYDROCHLORIC ACID
POLYVINYL ALCOHOL
POTASSIUM CHLORIDE
WATER
SODIUM CHLORIDE
SODIUM CITRATE, UNSPECIFIED FORM
SODIUM HYDROXIDE
THIMEROSAL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:24208-314-25 1 BOTTLE, DROPPER in 1 CARTON contains a BOTTLE, DROPPER
1 2.5 mL in 1 BOTTLE, DROPPER This package is contained within the CARTON (24208-314-25)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA074447 01/04/1995
Labeler — Bausch & Lomb Incorporated (196603781)
Establishment
Name Address ID/FEI Operations
Bausch & Lomb Incorporated 079587625 MANUFACTURE (24208-314)

Revised: 07/2016 Bausch & Lomb Incorporated

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