United States · FDA National Drug Code directory

Venlafaxine HCL ER

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: 72189-363_2c4c85cc-c2bb-ac98-e063-6294a90a973c
Product NDC: 72189-363
Form: CAPSULE, EXTENDED RELEASE
Composition / generic term: Venlafaxine HCL ER
Labeler: Direct_Rx
Marketing category: ANDA
Marketing start / end (source format): 20220622
Source listing expiry: 20261231

Source-listed ingredients

VENLAFAXINE HYDROCHLORIDE — 37.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-363-30) · 72189-363-30
60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-363-60) · 72189-363-60

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 →