United States · FDA National Drug Code directory
Venlafaxine Hydrochloride
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
- 80425-0396_19b15238-1c3c-6646-e063-6394a90a55bd
- Product NDC
- 80425-0396
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- VENLAFAXINE HYDROCHLORIDE
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240524
- Source listing expiry
- 20261231
Source-listed ingredients
- VENLAFAXINE HYDROCHLORIDE — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0396-1) · 80425-0396-1
- 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0396-2) · 80425-0396-2
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0396-3) · 80425-0396-3
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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