United States · FDA National Drug Code directory
Verapamil Hydrochloride
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
- 0591-2880_319554df-fc0d-428a-9799-a352100f1ce9
- Product NDC
- 0591-2880
- Form
- CAPSULE, DELAYED RELEASE PELLETS
- Composition / generic term
- verapamil hydrochloride
- Labeler
- Teva Pharmaceuticals Inc
- Marketing category
- NDA
- Marketing start / end (source format)
- 19900529 / 20260930
Source-listed ingredients
- VERAPAMIL HYDROCHLORIDE — 120 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0591-2880-01) · 0591-2880-01
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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