NDC 62559-275 – Nebivolol

Nebivolol Hydrochloride 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC62559-275

Product details

Brand name
Nebivolol
Generic name
Nebivolol
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203659
Marketed since
September 17, 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
62559-275-3030 TABLET in 1 BOTTLE (62559-275-30)Sep 17, 2021
62559-275-832300 TABLET in 1 BOTTLE (62559-275-83)Sep 17, 2021

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