LATANOPROST
- Product NDC
- 61919-112
- 11-digit product format
- 619190112
- Labeler code
- 61919
- Product ID
- 61919-112_9c9765a3-2068-5fe5-e053-2a95a90ab030
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LATANOPROST
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- DIRECT RX
- Application
- ANDA090887
- Marketing category
- ANDA
- Marketing start
- 2017-03-27
- 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
- 2021-12-31
- 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 |
|---|
| 61919-112-25 | LATANOPROST | 1 mL in 1 CARTON | SOLUTION/ DROPS | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-112 | LATANOPROST SOLUTION/ DROPS [DIRECT RX] | 2 | Legacy NDC, 1 package rows | 20200121_4bb5ec0f-317c-0992-e054-00144ff8d46c.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 |
|---|
| 61919-112-25 | 61919011225 | 1 mL in 1 CARTON (61919-112-25) | 1 ml | 2017-03-27 | 0000-00-00 | No | No | Current |