Travoprost Ophthalmic
- Product NDC
- 71335-2888
- 11-digit product format
- 713352888
- Labeler code
- 71335
- Product ID
- 71335-2888_436bca42-0e48-50ee-e063-6294a90ac16d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Travoprost Ophthalmic Solution
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203767
- Marketing category
- ANDA
- Marketing start
- 2021-04-15
- Substance
- TRAVOPROST
- Active strength
- .04 mg/mL
- Pharmacologic classes
- Prostaglandin Analog [EPC], Prostaglandins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data
- Finished product
- Yes
- Brand name base
- Travoprost Ophthalmic
- Listing expiration
- 2026-12-31
Active Ingredients
| Ingredient | Strength |
|---|
| TRAVOPROST | .04 mg/mL |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | WJ68R08KX9 |
| Rxcui | 284008 |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| WJ68R08KX9 | TRAVOPROST | 157283-68-6 | TRAVOPROST |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2888-1 | 71335288801 | 1 BOTTLE in 1 CARTON (71335-2888-1) / 2.5 mL in 1 BOTTLE | 1 bottle | 2021-04-15 | No | No | Current |