NDC 72205-336 – Ivabradine

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

Human Prescription Drug

Product NDC72205-336

Product details

Brand name
Ivabradine
Generic name
Ivabradine
Labeler
Novadoz Pharmaceuticals LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213483
Marketed since
April 28, 2025
Listing expires
December 31, 2027
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
72205-336-18180 TABLET, FILM COATED in 1 BOTTLE (72205-336-18)Jul 1, 2025
72205-336-6060 TABLET, FILM COATED in 1 BOTTLE (72205-336-60)Jul 1, 2025

Other Ivabradine products