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
- 0093-7295_3d07d8c6-ffea-41c3-a50c-4e3d723de14f
- Product NDC
- 0093-7295
- Form
- TABLET, FILM COATED
- Composition / generic term
- Carvedilol
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070906
- Source listing expiry
- 20261231
Source-listed ingredients
- CARVEDILOL — 12.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (0093-7295-01) · 0093-7295-01
- 500 TABLET, FILM COATED in 1 BOTTLE (0093-7295-05) · 0093-7295-05
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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