United States · FDA National Drug Code directory
Carvedilol Phosphate
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
- 71335-9707_0acb6c82-0308-4d04-b717-16acff5517ce
- Product NDC
- 71335-9707
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- Carvedilol Phosphate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171108
- Source listing expiry
- 20271231
Source-listed ingredients
- CARVEDILOL PHOSPHATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-9707-1) · 71335-9707-1
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-9707-2) · 71335-9707-2
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 →