Bivalirudin 70511-0142-84

Package NDC

70511-0142-84

Manufacturer: Maia Pharmaceuticals, Inc.
Dosage Form: Injection, Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: May 27, 2024
Listing Expires: December 31, 2026
Application: NDA211215

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Active Ingredients

Ingredient	Strength
Bivalirudin	250 mg/1

Drug Class

Anti-coagulant [EPC]Direct Thrombin Inhibitor [EPC]Anti-coagulant [EPC]

Selected Package

70511-0142-84Selected

10 VIAL, SINGLE-DOSE in 1 CARTON (70511-142-84) / 1 INJECTION, SOLUTION in 1 VIAL, SINGLE-DOSE

Other packages for this product(1)

70511-0142-50

1 VIAL, SINGLE-DOSE in 1 CARTON (70511-142-50) / 1 INJECTION, SOLUTION in 1 VIAL, SINGLE-DOSE

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