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
- 46708-792_e3e238db-4388-49bb-aa67-6d73adbb2280
- Product NDC
- 46708-792
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- VENLAFAXINE HYDROCHLORIDE
- Labeler
- Alembic Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240610
- 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 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-30) · 46708-792-30
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-31) · 46708-792-31
- 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-71) · 46708-792-71
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-90) · 46708-792-90
- 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-91) · 46708-792-91
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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