Latanoprost
- Product NDC
- 50090-7062
- 11-digit product format
- 500907062
- Labeler code
- 50090
- Product ID
- 50090-7062_85f8f5c2-da28-4c1e-b265-9723a6c6e8fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Latanoprost
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- ANDA091449
- Marketing category
- ANDA
- Marketing start
- 2011-01-07
- 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 |
|---|
| 50090-7062-0 | Latanoprost | 2.5 mL in 1 BOTTLE | SOLUTION | 2.5 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7062 | LATANOPROST SOLUTION [A-S MEDICATION SOLUTIONS] | 2 | Current NDC, 1 package rows | 20240229_8fb5edec-d94a-4aad-b42e-756267a3ae55.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7062-0 | 50090706200 | 2.5 mL in 1 BOTTLE (50090-7062-0) | 2.5 ml | 2024-01-16 | No | No | Current |