Latanoprost
- Product NDC
- 65862-872
- 11-digit product format
- 658620872
- Labeler code
- 65862
- Product ID
- 65862-872_cad9da15-f479-4b42-9d22-02c3f7dab1ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Latanoprost
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA206519
- Marketing category
- ANDA
- Marketing start
- 2019-09-03
- 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 |
|---|
| 65862-872-25 | Latanoprost | 2.5 mL in 1 BOTTLE | SOLUTION/ DROPS | 2.5 | | 5 |
| 65862-872-25 | Latanoprost | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65862-872 | LATANOPROST SOLUTION/ DROPS [AUROBINDO PHARMA LIMITED] | 5 | Current NDC, Legacy NDC, 2 package rows | 20240929_19cdfef0-b770-4758-8f59-1769e4b6119c.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 |
|---|
| 65862-872-25 | 65862087225 | 1 BOTTLE in 1 CARTON (65862-872-25) / 2.5 mL in 1 BOTTLE | 1 bottle | 2019-09-03 | 0000-00-00 | No | No | Current |