NDC 62559-277 – Nebivolol

Nebivolol Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC62559-277

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 (3)

Package NDCDescriptionSince
62559-277-05500 TABLET in 1 BOTTLE (62559-277-05)Sep 17, 2021
62559-277-3030 TABLET in 1 BOTTLE (62559-277-30)Sep 17, 2021
62559-277-9090 TABLET in 1 BOTTLE (62559-277-90)Sep 17, 2021

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