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
- 71335-9704_1471508e-7fe4-43db-94ea-b4df1bcbafa9
- Product NDC
- 71335-9704
- 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 — 37.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-9704-1) · 71335-9704-1
- 60 TABLET in 1 BOTTLE (71335-9704-2) · 71335-9704-2
- 90 TABLET in 1 BOTTLE (71335-9704-3) · 71335-9704-3
- 10 TABLET in 1 BOTTLE (71335-9704-4) · 71335-9704-4
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 →