Dipyridamole
- Product NDC
- 0527-1462
- 11-digit product format
- 005271462
- Labeler code
- 0527
- Product ID
- 0527-1462_c8c9bc23-afe1-4cde-aed0-64f3d21b94f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dipyridamole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA040898
- Marketing category
- ANDA
- Marketing start
- 2008-04-23
- Marketing end
- 0000-00-00
- Substance
- DIPYRIDAMOLE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Decreased Platelet Aggregation [PE], Platelet Aggregation Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0527-1462-01 | 00527146201 | 100 TABLET, FILM COATED in 1 BOTTLE (0527-1462-01) | 2008-04-23 | 0000-00-00 | No | No | Current |
| 0527-1462-05 | 00527146205 | 500 TABLET, FILM COATED in 1 BOTTLE (0527-1462-05) | 2008-04-23 | 0000-00-00 | No | No | Current |
| 0527-1462-10 | 00527146210 | 1000 TABLET, FILM COATED in 1 BOTTLE (0527-1462-10) | 2008-04-23 | 0000-00-00 | No | No | Current |