Drug Atlas

NDC 42291-874 – Nebivolol

Nebivolol Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC42291-874

Product details

Brand name: Nebivolol
Generic name: Nebivolol hydrochloride
Labeler: AvKARE
Dosage form: Tablet
Route: Oral
Marketing category: ANDA · ANDA203821
Marketed since: July 10, 2024
Listing expires: December 31, 2027
Pharmacologic class: beta-Adrenergic Blocker

Active ingredients

Nebivolol Hydrochloride 20 mg/1

Uses, dosage, side effects and warnings for Nebivolol →

Package NDC codes (1)

Package NDC	Description	Since
42291-874-90	90 TABLET in 1 BOTTLE (42291-874-90)	Jul 10, 2024

Recalls mentioning this NDC

D-0222-2026 Dec 17, 2025 · Class III
Cross Contamination with Other Products

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