LATANOPROST
- Product NDC
- 50090-1240
- 11-digit product format
- 500901240
- Labeler code
- 50090
- Product ID
- 50090-1240_dc59eec6-cc4c-473c-a7a8-ee2c08f9e008
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LATANOPROST
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- ANDA090887
- Marketing category
- ANDA
- Marketing start
- 2012-07-01
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record