NDC 50090-5708 – Nebivolol

Nebivolol Hydrochloride 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-5708

Product details

Brand name
Nebivolol
Generic name
Nebivolol
Labeler
A-S Medication Solutions
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203828
Marketed since
September 16, 2021
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nebivolol →

Package NDC codes (2)

Package NDCDescriptionSince
50090-5708-05 TABLET in 1 BOTTLE (50090-5708-0)Sep 23, 2021
50090-5708-190 TABLET in 1 BOTTLE (50090-5708-1)Oct 7, 2021

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