NDC 67877-391 – Nebivolol

Nebivolol Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC67877-391

Product details

Brand name
Nebivolol
Generic name
Nebivolol
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203828
Marketed since
September 16, 2021
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nebivolol →

Package NDC codes (4)

Package NDCDescriptionSince
67877-391-01100 TABLET in 1 BOTTLE (67877-391-01)Sep 16, 2021
67877-391-3030 TABLET in 1 BOTTLE (67877-391-30)Sep 16, 2021
67877-391-331 BLISTER PACK in 1 CARTON (67877-391-33) / 10 TABLET in 1 BLISTER PACKSep 16, 2021
67877-391-9090 TABLET in 1 BOTTLE (67877-391-90)Sep 16, 2021

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