NDC 70756-293 – Nebivolol

Nebivolol Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70756-293

Product details

Brand name
Nebivolol
Generic name
Nebivolol
Labeler
Lifestar Pharma LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA216172
Marketed since
November 14, 2022
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
70756-293-3030 TABLET in 1 BOTTLE (70756-293-30)Nov 14, 2022
70756-293-9090 TABLET in 1 BOTTLE (70756-293-90)Nov 14, 2022

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