Latanoprost
- Product NDC
- 13985-610
- 11-digit product format
- 139850610
- Labeler code
- 13985
- Product ID
- 13985-610_5b811738-4fd3-4ac2-ad21-05f0fe1cbbe0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Latanoprost
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- MWI
- Application
- ANDA090887
- Marketing category
- ANDA
- Marketing start
- 2015-04-08
- Marketing end
- 2021-09-01
- Substance
- LATANOPROST
- Active strength
- 50 ug/mL
- Pharmacologic classes
- Prostaglandin Analog [EPC],Prostaglandins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 13985-610-02 | 13985061002 | 1 BOTTLE, DROPPER in 1 CARTON (13985-610-02) > 2.5 mL in 1 BOTTLE, DROPPER | 2015-04-08 | 2021-09-01 | No | No | Current |