Travoprost Ophthalmic Solution

Product NDC
0781-6185
11-digit product format
007816185
Labeler code
0781
Product ID
0781-6185_85482fff-ce5d-449c-9bee-883e52713d6e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
travoprost
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Sandoz Inc
Application
NDA021994
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2019-12-18
Marketing end
0000-00-00
Substance
TRAVOPROST
Active strength
0 mg/mL
Pharmacologic classes
Prostaglandin Analog [EPC],Prostaglandins [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
c9a16692-b67d-fe7d-e549-d5c422428aa8Product name520250305
d244df75-ee9e-4580-9b0c-1e61287c8253Product name120250102
52ddd23e-485b-499f-9fa1-f86549f4d9c0Product name220200605

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-6185-56ML - Milliliter0781-6185da76b21a-abda-444d-8633-1ca96ac3174e12020-01-03
0781-6185-75ML - Milliliter0781-618558a8ef37-d1eb-4d01-8ff0-740551dd414412020-01-03

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0781-6185TRAVOPROST OPHTHALMIC SOLUTION (TRAVOPROST) SOLUTION/ DROPS [SANDOZ INC]4Legacy NDC20250312_c17aa704-1ec6-4610-a448-4964bdb1cba1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0781-6185-56007816185561 BOTTLE in 1 CARTON (0781-6185-56) > 2.5 mL in 1 BOTTLE1 bottle2019-12-180000-00-00NoNoCurrent
0781-6185-75007816185751 BOTTLE in 1 CARTON (0781-6185-75) > 5 mL in 1 BOTTLE1 bottle2019-12-180000-00-00NoNoCurrent