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
- 63187-941_f83cec53-93fb-4fa6-81e8-5e8801c99e62
- Product NDC
- 63187-941
- Form
- TABLET, FILM COATED
- Composition / generic term
- Carvedilol
- Labeler
- Proficient Rx LP
- 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
- 30 TABLET, FILM COATED in 1 BOTTLE (63187-941-30) · 63187-941-30
- 60 TABLET, FILM COATED in 1 BOTTLE (63187-941-60) · 63187-941-60
- 90 TABLET, FILM COATED in 1 BOTTLE (63187-941-90) · 63187-941-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →