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
- 71335-2709_ba34434b-98f0-4bb0-946a-fd3f768345f2
- Product NDC
- 71335-2709
- Form
- TABLET
- Composition / generic term
- Venlafaxine
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080613
- Source listing expiry
- 20261231
Source-listed ingredients
- VENLAFAXINE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-2709-1) · 71335-2709-1
- 60 TABLET in 1 BOTTLE (71335-2709-2) · 71335-2709-2
- 90 TABLET in 1 BOTTLE (71335-2709-3) · 71335-2709-3
- 18 TABLET in 1 BOTTLE (71335-2709-4) · 71335-2709-4
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →