NDC 70518-3527 – Nebivolol

Nebivolol Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-3527

Product details

Brand name
Nebivolol
Generic name
Nebivolol
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203828
Marketed since
September 20, 2022
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nebivolol →

Package NDC codes (1)

Package NDCDescriptionSince
70518-3527-090 TABLET in 1 BOTTLE, PLASTIC (70518-3527-0)Sep 20, 2022

Other Nebivolol products