NDC 50742-363 – Ivabradine

Ivabradine Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50742-363

Product details

Brand name
Ivabradine
Generic name
Ivabradine
Labeler
Ingenus Pharmaceuticals, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA214051
Marketed since
July 15, 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 (1)

Package NDCDescriptionSince
50742-363-6060 TABLET, FILM COATED in 1 BOTTLE (50742-363-60)Jul 15, 2024

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