United States · FDA National Drug Code directory

vilazodone 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
82804-128_f68720fd-9122-4922-b472-733da8bd0a00
Product NDC
82804-128
Form
TABLET
Composition / generic term
vilazodone hydrochloride
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20231026
Source listing expiry
20261231

Source-listed ingredients

  • VILAZODONE HYDROCHLORIDE — 40 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (82804-128-30) · 82804-128-30

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.

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