Latanoprost
- Product NDC
- 25021-001
- 11-digit product format
- 250210001
- Labeler code
- 25021
- Product ID
- 25021-001_8ce78c02-d0b0-4629-b51d-0c674c6e2e43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Latanoprost
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA218257
- Marketing category
- ANDA
- Marketing start
- 2025-07-15
- Substance
- LATANOPROST
- Active strength
- 50 ug/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Latanoprost
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LATANOPROST | 50 ug/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6Z5B6HVF6O |
| Rxcui | 314072 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 25021-001-02 | Latanoprost | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 1 |
| 25021-001-02 | Latanoprost | 2.5 mL in 1 BOTTLE | SOLUTION/ DROPS | 2.5 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 25021-001-02 | 25021000102 | 1 BOTTLE in 1 CARTON (25021-001-02) / 2.5 mL in 1 BOTTLE | 1 bottle | 2025-07-15 | No | No | Historical |