NDC 31722-588 – Nebivolol

Nebivolol Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC31722-588

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
31722-588-01100 TABLET in 1 BOTTLE (31722-588-01)Sep 17, 2021
31722-588-3030 TABLET in 1 BOTTLE (31722-588-30)Sep 17, 2021
31722-588-3210 BLISTER PACK in 1 CARTON (31722-588-32) / 10 TABLET in 1 BLISTER PACK (31722-588-31)Sep 17, 2021
31722-588-3418 BLISTER PACK in 1 CARTON (31722-588-34) / 7 TABLET in 1 BLISTER PACK (31722-588-33)Sep 17, 2021
31722-588-9090 TABLET in 1 BOTTLE (31722-588-90)Sep 17, 2021

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