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
- 65841-753_f20749dc-d1f6-4860-b583-82b82d3a2242
- Product NDC
- 65841-753
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- venlafaxine hydrochloride
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110601
- Source listing expiry
- 20261231
Source-listed ingredients
- VENLAFAXINE HYDROCHLORIDE — 150 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-06) · 65841-753-06
- 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-10) · 65841-753-10
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-16) · 65841-753-16
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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