United States · FDA National Drug Code directory
Carvedilol
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
- 71335-1623_35711bc7-16ba-4eb1-9ccc-b8e1bcf67ccd
- Product NDC
- 71335-1623
- Form
- TABLET, FILM COATED
- Composition / generic term
- Carvedilol
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070905
- Source listing expiry
- 20271231
Source-listed ingredients
- CARVEDILOL — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-1623-1) · 71335-1623-1
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1623-2) · 71335-1623-2
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1623-3) · 71335-1623-3
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1623-4) · 71335-1623-4
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-1623-5) · 71335-1623-5
- 180 TABLET, FILM COATED in 1 BOTTLE (71335-1623-6) · 71335-1623-6
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-1623-7) · 71335-1623-7
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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