United States · FDA National Drug Code directory

Desvenlafaxine 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
72189-567_34f5586c-4441-54fb-e063-6394a90aa90d
Product NDC
72189-567
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Desvenlafaxine ER
Labeler
Direct_rx
Marketing category
ANDA
Marketing start / end (source format)
20240718
Source listing expiry
20261231

Source-listed ingredients

  • DESVENLAFAXINE SUCCINATE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-567-28) · 72189-567-28
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-567-30) · 72189-567-30
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-567-60) · 72189-567-60

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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