United States · FDA National Drug Code directory
DESVENLAFAXINE
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
- 72603-556_34888df6-f68d-c171-e063-6294a90a7604
- Product NDC
- 72603-556
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- DESVENLAFAXINE
- Labeler
- NorthStar Rx LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250502
- Source listing expiry
- 20261231
Source-listed ingredients
- DESVENLAFAXINE SUCCINATE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, EXTENDED RELEASE in 1 PACKAGE (72603-556-01) · 72603-556-01
- 90 TABLET, EXTENDED RELEASE in 1 PACKAGE (72603-556-02) · 72603-556-02
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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