United States · FDA National Drug Code directory

Venlafaxine

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: 72241-075_14b38374-7287-47dd-8ef9-e88bd5b23a26
Product NDC: 72241-075
Form: TABLET, COATED
Composition / generic term: Venlafaxine
Labeler: Modavar Pharmaceuticals LLC
Marketing category: ANDA
Marketing start / end (source format): 20180105
Source listing expiry: 20261231

Source-listed ingredients

VENLAFAXINE HYDROCHLORIDE — 75 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

90 TABLET, COATED in 1 BOTTLE (72241-075-04) · 72241-075-04
1000 TABLET, COATED in 1 BOTTLE (72241-075-11) · 72241-075-11
30 TABLET, COATED in 1 BOTTLE (72241-075-22) · 72241-075-22

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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