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
0378-6440_c63ca9bc-5c77-4e53-8adf-9cfd16bfe012
Product NDC
0378-6440
Form
CAPSULE, EXTENDED RELEASE
Composition / generic term
verapamil hydrochloride
Labeler
Mylan Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
19990520
Source listing expiry
20261231

Source-listed ingredients

  • VERAPAMIL HYDROCHLORIDE — 240 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-6440-01) · 0378-6440-01

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 →