Details for New Drug Application (NDA): 213947
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The generic ingredient in TIROFIBAN HYDROCHLORIDE is tirofiban hydrochloride. There are four drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the tirofiban hydrochloride profile page.
Summary for 213947
| Tradename: | TIROFIBAN HYDROCHLORIDE |
| Applicant: | Nexus |
| Ingredient: | tirofiban hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 213947
| Physiological Effect | Decreased Platelet Aggregation |
Suppliers and Packaging for NDA: 213947
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| TIROFIBAN HYDROCHLORIDE | tirofiban hydrochloride | SOLUTION;INTRAVENOUS | 213947 | ANDA | Nexus Pharmaceuticals LLC | 14789-101 | 14789-101-01 | 1 BAG in 1 CARTON (14789-101-01) / 100 mL in 1 BAG |
| TIROFIBAN HYDROCHLORIDE | tirofiban hydrochloride | SOLUTION;INTRAVENOUS | 213947 | ANDA | Nexus Pharmaceuticals LLC | 14789-102 | 14789-102-02 | 1 BAG in 1 CARTON (14789-102-02) / 250 mL in 1 BAG |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | EQ 5MG BASE/100ML (EQ 0.05MG BASE/ML) | ||||
| Approval Date: | Feb 7, 2023 | TE: | AP | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | EQ 12.5MG BASE/250ML (EQ 0.05MG BASE/ML) | ||||
| Approval Date: | Jul 24, 2023 | TE: | AP | RLD: | No | ||||
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