Prasugrel
- Product NDC
- 50090-4118
- 11-digit product format
- 500904118
- Labeler code
- 50090
- Product ID
- 50090-4118_94849f6a-f521-4daf-949b-231cab730dce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prasugrel
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA205913
- Marketing category
- ANDA
- Marketing start
- 2018-06-22
- Marketing end
- 0000-00-00
- 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
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4118-0 | 50090411800 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-4118-0) | 2019-02-02 | 0000-00-00 | No | No | Current |