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
- 47335-759_dae15132-d26b-4ea9-b937-da9c282ada48
- Product NDC
- 47335-759
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Venlafaxine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141215
- Source listing expiry
- 20261231
Source-listed ingredients
- VENLAFAXINE HYDROCHLORIDE — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-08) · 47335-759-08
- 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-18) · 47335-759-18
- 10 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-759-61) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 47335-759-61
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-81) · 47335-759-81
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-83) · 47335-759-83
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-88) · 47335-759-88
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 →