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
- 72205-153_e54ddb53-542b-4183-8950-5b3947ecead0
- Product NDC
- 72205-153
- Form
- TABLET
- Composition / generic term
- NEBIVOLOL
- Labeler
- Novadoz Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241001
- Source listing expiry
- 20261231
Source-listed ingredients
- NEBIVOLOL HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (72205-153-30) · 72205-153-30
- 90 TABLET in 1 BOTTLE (72205-153-90) · 72205-153-90
- 100 TABLET in 1 BOTTLE (72205-153-91) · 72205-153-91
- 100 TABLET in 1 BOX, UNIT-DOSE (72205-153-99) · 72205-153-99
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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