NDC 33342-459 – Nebivolol

Nebivolol Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC33342-459

Product details

Brand name
Nebivolol
Generic name
Nebivolol
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212661
Marketed since
January 29, 2025
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
33342-459-0730 TABLET in 1 BOTTLE (33342-459-07)Jan 29, 2025
33342-459-1090 TABLET in 1 BOTTLE (33342-459-10)Jan 29, 2025
33342-459-2512 BLISTER PACK in 1 CARTON (33342-459-25) / 10 TABLET in 1 BLISTER PACKJan 29, 2025

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