NDC 70518-4648 – Nebivolol

Nebivolol Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-4648

Product details

Brand name
Nebivolol
Generic name
Nebivolol
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA217397
Marketed since
April 28, 2026
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nebivolol →

Package NDC codes (1)

Package NDCDescriptionSince
70518-4648-050 POUCH in 1 BOX (70518-4648-0) / 1 TABLET in 1 POUCH (70518-4648-1)Apr 28, 2026

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