Travatan Z (Page 3 of 3)

PRINCIPAL DISPLAY PANEL

NDC 0078-0946-25

Rx Only

TRAVATAN Z®

(travoprost ophthalmic solution) 0.004%

5 mL
STERILE

NOVARTIS

PRINCIPAL DISPLAY PANEL
								NDC 0078-0946-25
								Rx Only
								TRAVATAN Z®
								(travoprost ophthalmic solution) 0.004%
								5 mL
								STERILE
								NOVARTIS
(click image for full-size original)
TRAVATAN Z
travoprost solution/ drops
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0078-0946
Route of Administration OPHTHALMIC DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRAVOPROST (TRAVOPROST) TRAVOPROST 0.04 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
POLYOXYL 40 CASTOR OIL
BORIC ACID
PROPYLENE GLYCOL
SORBITOL
ZINC CHLORIDE
SODIUM HYDROXIDE
HYDROCHLORIC ACID
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0078-0946-40 1 BOTTLE in 1 CARTON contains a BOTTLE
1 2.5 mL in 1 BOTTLE This package is contained within the CARTON (0078-0946-40)
2 NDC:0078-0946-25 1 BOTTLE in 1 CARTON contains a BOTTLE
2 5 mL in 1 BOTTLE This package is contained within the CARTON (0078-0946-25)
3 NDC:0078-0946-98 1 BOTTLE in 1 CARTON contains a BOTTLE
3 2.5 mL in 1 BOTTLE This package is contained within the CARTON (0078-0946-98)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA021994 10/20/2006
Labeler — Novartis Pharmaceuticals Corporation (002147023)

Revised: 05/2020 Novartis Pharmaceuticals Corporation

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