Cilostazol
- Product NDC
- 68071-2065
- 11-digit product format
- 680712065
- Labeler code
- 68071
- Product ID
- 68071-2065_46dff4c0-9a2d-20f9-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cilostazol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077021
- Marketing category
- ANDA
- Marketing start
- 2004-11-23
- Marketing end
- 0000-00-00
- Substance
- CILOSTAZOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Phosphodiesterase 3 Inhibitor [EPC],Phosphodiesterase 3 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record