Latanoprost
- Product NDC
- 71205-154
- 11-digit product format
- 712050154
- Labeler code
- 71205
- Product ID
- 71205-154_b8f1a9ff-491b-4743-8b06-76c9a6de13b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- latanoprost
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Proficient Rx LP
- Application
- ANDA201006
- Marketing category
- ANDA
- Marketing start
- 2011-03-22
- 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 |
|---|
| 71205-154-25 | Latanoprost | 2.5 mL in 1 BOTTLE | SOLUTION/ DROPS | 2.5 | | 6 |
| 71205-154-25 | Latanoprost | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-154 | LATANOPROST SOLUTION/ DROPS [PROFICIENT RX LP] | 6 | Current NDC, Legacy NDC, 2 package rows | 20241019_bfd773ed-c461-4732-b1ba-0c240f3fdae0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-154-25 | 71205015425 | 1 BOTTLE in 1 CARTON (71205-154-25) / 2.5 mL in 1 BOTTLE | 1 bottle | 2018-11-01 | 0000-00-00 | No | No | Current |