Prasugrel
- Product NDC
- 51407-248
- 11-digit product format
- 514070248
- Labeler code
- 51407
- Product ID
- 51407-248_dc7991c8-6d60-2f59-e053-2a95a90acfdb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prasugrel
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA205897
- Marketing category
- ANDA
- Marketing start
- 2017-10-16
- Marketing end
- 2022-06-30
- Substance
- PRASUGREL HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Decreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-248-30 | 51407024830 | 30 TABLET, FILM COATED in 1 BOTTLE (51407-248-30) | 2020-01-17 | 0000-00-00 | No | No | Current |