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
- 50090-2119_adb37b64-cfc9-4575-b0c2-c449c0b38799
- Product NDC
- 50090-2119
- Form
- TABLET, FILM COATED
- Composition / generic term
- Carvedilol
- Labeler
- A-S Medication Solutions
- 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
- 60 TABLET, FILM COATED in 1 BOTTLE (50090-2119-0) · 50090-2119-0
- 180 TABLET, FILM COATED in 1 BOTTLE (50090-2119-1) · 50090-2119-1
- 90 TABLET, FILM COATED in 1 BOTTLE (50090-2119-3) · 50090-2119-3
- 30 TABLET, FILM COATED in 1 BOTTLE (50090-2119-4) · 50090-2119-4
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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