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
- 52427-632_1b0762be-0db0-b997-b76b-b212a496f82c
- Product NDC
- 52427-632
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- venlafaxine
- Labeler
- Almatica Pharma LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20220630
- Source listing expiry
- 20261231
Source-listed ingredients
- VENLAFAXINE BESYLATE MONOHYDRATE — 112.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (52427-632-30) · 52427-632-30
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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