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
- 68788-9790_a8cb0f54-4ce5-488f-a49a-8e7b182b7041
- Product NDC
- 68788-9790
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Verapamil Hydrochloride
- Labeler
- Preferred Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120604
- Source listing expiry
- 20261231
Source-listed ingredients
- VERAPAMIL HYDROCHLORIDE — 240 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-9790-1) · 68788-9790-1
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-9790-3) · 68788-9790-3
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-9790-6) · 68788-9790-6
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-9790-9) · 68788-9790-9
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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