Persantine
- Product NDC
- 0597-0017
- 11-digit product format
- 005970017
- Labeler code
- 0597
- Product ID
- 0597-0017_b91f02b7-092e-35b9-b4d9-8a1a47cbf843
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dipyridamole
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Boehringer Ingelheim Pharmaceuticals, Inc.
- Application
- NDA012836
- Marketing category
- NDA
- Marketing start
- 1999-06-01
- Marketing end
- 0000-00-00
- Substance
- DIPYRIDAMOLE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 0597-0017-01 | 00597001701 | 100 TABLET, COATED in 1 BOTTLE (0597-0017-01) | 1999-06-01 | 0000-00-00 | No | No | Current |