NDC 50090-7853 – Nebivolol

Nebivolol Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-7853

Product details

Brand name
Nebivolol
Generic name
Nebivolol
Labeler
A-S Medication Solutions
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA217397
Marketed since
October 1, 2024
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nebivolol →

Package NDC codes (2)

Package NDCDescriptionSince
50090-7853-130 TABLET in 1 BOTTLE (50090-7853-1)Jan 8, 2026
50090-7853-290 TABLET in 1 BOTTLE (50090-7853-2)Jan 8, 2026

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