Dipyridamole
- Product NDC
- 62559-237
- 11-digit product format
- 625590237
- Labeler code
- 62559
- Product ID
- 62559-237_162b7dd5-8490-4010-9ede-1d559633367f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dipyridamole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA086944
- Marketing category
- ANDA
- Marketing start
- 2021-11-22
- Marketing end
- 0000-00-00
- Substance
- DIPYRIDAMOLE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62559-237-01 | 62559023701 | 100 TABLET, FILM COATED in 1 BOTTLE (62559-237-01) | 2021-11-22 | 0000-00-00 | No | No | Current |