Strength
7.5 mg/1
Manufacturer
Zydus Pharmaceuticals (USA) Inc.NDC
70710147206
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
IVABRADINE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA213442On Market Since
7/2/2024
Pharmacological Classes
Hyperpolarization-activated Cyclic Nucleotide-gated Channel Antagonists
Hyperpolarization-activated Cyclic Nucleotide-gated Channel Blocker
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