United States · FDA National Drug Code directory
Nebivolol
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 67877-391_4f315a54-2598-4463-8884-0b643e86f8c0
- Product NDC
- 67877-391
- Form
- TABLET
- Composition / generic term
- Nebivolol
- Labeler
- Ascend Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210916
- Source listing expiry
- 20261231
Source-listed ingredients
- NEBIVOLOL HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (67877-391-01) · 67877-391-01
- 30 TABLET in 1 BOTTLE (67877-391-30) · 67877-391-30
- 1 BLISTER PACK in 1 CARTON (67877-391-33) / 10 TABLET in 1 BLISTER PACK · 67877-391-33
- 90 TABLET in 1 BOTTLE (67877-391-90) · 67877-391-90
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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