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
- 68462-162_5f5b2d20-cc2a-4e91-b2b9-260e7438ab2c
- Product NDC
- 68462-162
- Form
- TABLET, FILM COATED
- Composition / generic term
- Carvedilol
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070905
- Source listing expiry
- 20261231
Source-listed ingredients
- CARVEDILOL — 3.125 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (68462-162-01) · 68462-162-01
- 500 TABLET, FILM COATED in 1 BOTTLE (68462-162-05) · 68462-162-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (68462-162-10) · 68462-162-10
- 180 TABLET, FILM COATED in 1 BOTTLE (68462-162-18) · 68462-162-18
- 60 TABLET, FILM COATED in 1 BOTTLE (68462-162-60) · 68462-162-60
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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