NDC 72241-033 – Nebivolol

Nebivolol Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72241-033

Product details

Brand name
Nebivolol
Generic name
Nebivolol
Labeler
Modavar Pharmaceuticals LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208717
Marketed since
December 29, 2017
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nebivolol →

Package NDC codes (4)

Package NDCDescriptionSince
72241-033-0490 TABLET in 1 BOTTLE (72241-033-04)Dec 18, 2021
72241-033-05100 TABLET in 1 BOTTLE (72241-033-05)Dec 18, 2021
72241-033-111000 TABLET in 1 BOTTLE (72241-033-11)Dec 18, 2021
72241-033-2230 TABLET in 1 BOTTLE (72241-033-22)Dec 18, 2021

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