Latanoprost
- Product NDC
- 68071-1683
- 11-digit product format
- 680711683
- Labeler code
- 68071
- Product ID
- 68071-1683_5e9762d8-cc50-9f18-e053-2991aa0a14bd
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record