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
- 70518-0605_55677a13-4a6f-f955-e063-6394a90a78a2
- Product NDC
- 70518-0605
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- verapamil hydrochloride
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170703
- Source listing expiry
- 20271231
Source-listed ingredients
- VERAPAMIL HYDROCHLORIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 POUCH in 1 BOX (70518-0605-2) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-0605-3) · 70518-0605-2
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 →