Latanoprost
- Product NDC
- 68071-3884
- 11-digit product format
- 680713884
- Labeler code
- 68071
- Product ID
- 68071-3884_3c477d33-a8ca-d39f-e063-6294a90ac5f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Latanoprost
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- NuCare Pharmaceuticals, Inc.
- 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 |
|---|
| 68071-3884-2 | 68071388402 | 1 BOTTLE in 1 CARTON (68071-3884-2) / 2.5 mL in 1 BOTTLE | 1 bottle | 2025-08-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Latanoprost | NuCare Pharmaceuticals, Inc. | 2025-08-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |