Details for New Drug Application (NDA): 205888
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The generic ingredient in PRASUGREL is prasugrel hydrochloride. There are nineteen drug master file entries for this compound. Nine suppliers are listed for this compound. Additional details are available on the prasugrel hydrochloride profile page.
Summary for 205888
Tradename: | PRASUGREL |
Applicant: | Aurobindo Pharma |
Ingredient: | prasugrel hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 205888
Mechanism of Action | P2Y12 Receptor Antagonists |
Physiological Effect | Decreased Platelet Aggregation |
Medical Subject Heading (MeSH) Categories for 205888
Suppliers and Packaging for NDA: 205888
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PRASUGREL | prasugrel hydrochloride | TABLET;ORAL | 205888 | ANDA | Aurobindo Pharma Limited | 65862-829 | 65862-829-03 | 3 BLISTER PACK in 1 CARTON (65862-829-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-829-10) |
PRASUGREL | prasugrel hydrochloride | TABLET;ORAL | 205888 | ANDA | Aurobindo Pharma Limited | 65862-829 | 65862-829-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-829-30) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 5MG BASE | ||||
Approval Date: | Oct 16, 2017 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 10MG BASE | ||||
Approval Date: | Oct 16, 2017 | TE: | AB | RLD: | No |
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