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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6Z5B6HVF6O | LATANOPROST | 130209-82-4 | LATANOPROST |
Packages
| 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 | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Latanoprost | A-S Medication Solutions | 2024-02-27 | HUMAN PRESCRIPTION DRUG LABEL | 2 |