Latanoprost
- Product NDC
- 68071-4650
- 11-digit product format
- 680714650
- Labeler code
- 68071
- Product ID
- 68071-4650_bb8b6493-f6a2-2632-e053-2a95a90afe51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- latanoprost
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA201006
- Marketing category
- ANDA
- Marketing start
- 2011-03-22
- Marketing end
- 0000-00-00
- Substance
- LATANOPROST
- Active strength
- 50 ug/mL
- Pharmacologic classes
- Prostaglandin Analog [EPC],Prostaglandins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-4650-2 | Latanoprost | 2.5 mL in 1 BOTTLE | SOLUTION/ DROPS | 2.5 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-4650 | LATANOPROST SOLUTION/ DROPS [NUCARE PHARMACEUTICALS,INC.] | 3 | Legacy NDC, 1 package rows | 20210218_7c3ba2a5-54c9-e76b-e053-2a91aa0a891f.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 |
|---|
| 68071-4650-2 | 68071465002 | 2.5 mL in 1 BOTTLE (68071-4650-2) | 2.5 ml | 2018-12-04 | 0000-00-00 | No | No | Current |