Cilostazol
- Product NDC
- 70518-2208
- 11-digit product format
- 705182208
- Labeler code
- 70518
- Product ID
- 70518-2208_c703108f-36e8-0c99-e053-2a95a90ad1ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cilostazol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077027
- Marketing category
- ANDA
- Marketing start
- 2019-07-11
- Marketing end
- 0000-00-00
- Substance
- CILOSTAZOL
- Active strength
- 50 mg/1
- Pharmacologic classes
- Phosphodiesterase 3 Inhibitor [EPC],Phosphodiesterase 3 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2208-0 | 70518220800 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2208-0) | 90 tablet | 2019-07-11 | 0000-00-00 | No | No | Current |