Cilostazol
- Product NDC
- 0185-0123
- 11-digit product format
- 001850123
- Labeler code
- 0185
- Product ID
- 0185-0123_05a33095-18cb-4628-811d-ba56f7e07820
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cilostazol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Eon Labs, Inc.
- Application
- ANDA077310
- Marketing category
- ANDA
- Marketing start
- 2005-11-08
- Marketing end
- 2021-05-31
- Substance
- CILOSTAZOL
- Active strength
- 50 mg/1
- Pharmacologic classes
- Phosphodiesterase 3 Inhibitor [EPC],Phosphodiesterase 3 Inhibitors [MoA]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0185-0123-60 | 00185012360 | 60 TABLET in 1 BOTTLE (0185-0123-60) | 60 tablet | 2005-11-08 | 2021-05-31 | No | No | Current |