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
- 75834-320_f81979a5-e2d6-4eae-a427-b8c125a3a1e3
- Product NDC
- 75834-320
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- VERAPAMIL HYDROCHLORIDE
- Labeler
- Nivagen Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230102
- Source listing expiry
- 20271231
Source-listed ingredients
- VERAPAMIL HYDROCHLORIDE — 120 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (75834-320-01) · 75834-320-01
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (75834-320-05) · 75834-320-05
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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