NDC 31722-586 – Nebivolol

Nebivolol Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC31722-586

Product details

Brand name
Nebivolol
Generic name
Nebivolol
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203825
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 (5)

Package NDCDescriptionSince
31722-586-01100 TABLET in 1 BOTTLE (31722-586-01)Sep 17, 2021
31722-586-3030 TABLET in 1 BOTTLE (31722-586-30)Sep 17, 2021
31722-586-3210 BLISTER PACK in 1 CARTON (31722-586-32) / 10 TABLET in 1 BLISTER PACK (31722-586-31)Sep 17, 2021
31722-586-3418 BLISTER PACK in 1 CARTON (31722-586-34) / 7 TABLET in 1 BLISTER PACK (31722-586-33)Sep 17, 2021
31722-586-9090 TABLET in 1 BOTTLE (31722-586-90)Sep 17, 2021

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