NDC 62332-679 – Ivabradine

Ivabradine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC62332-679

Product details

Brand name
Ivabradine
Generic name
Ivabradine
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215238
Marketed since
December 20, 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
62332-679-45180 TABLET, FILM COATED in 1 BOTTLE (62332-679-45)Dec 20, 2024
62332-679-6060 TABLET, FILM COATED in 1 BOTTLE (62332-679-60)Dec 20, 2024

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