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: 71205-017_a56062ad-d6ec-4335-b902-7ac80cecf3d4
Product NDC: 71205-017
Form: TABLET, FILM COATED, EXTENDED RELEASE
Composition / generic term: verapamil hydrochloride
Labeler: Proficient Rx LP
Marketing category: ANDA
Marketing start / end (source format): 20090917
Source listing expiry: 20261231

Source-listed ingredients

VERAPAMIL HYDROCHLORIDE — 240 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-017-30) · 71205-017-30
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-017-60) · 71205-017-60
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-017-90) · 71205-017-90

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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