NDC 70710-1472 – Ivabradine

Ivabradine Hydrochloride 7.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70710-1472

Product details

Brand name
Ivabradine
Generic name
Ivabradine
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213442
Marketed since
July 2, 2024
Listing expires
December 31, 2026
Pharmacologic class
Hyperpolarization-activated Cyclic Nucleotide-gated Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Ivabradine →

Package NDC codes (2)

Package NDCDescriptionSince
70710-1472-660 TABLET in 1 BOTTLE (70710-1472-6)Jul 2, 2024
70710-1472-8180 TABLET in 1 BOTTLE (70710-1472-8)Jul 2, 2024

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