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
- 24658-127_9478c4cb-36bd-48e8-85e4-d1a8af15f39c
- Product NDC
- 24658-127
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- VENLAFAXINE HYDROCHLORIDE
- Labeler
- PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260728
- Source listing expiry
- 20271231
Source-listed ingredients
- VENLAFAXINE HYDROCHLORIDE — 150 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24658-127-05) · 24658-127-05
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24658-127-30) · 24658-127-30
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24658-127-90) · 24658-127-90
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 →