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
- 70710-1698_9d291423-f1d9-4605-af7c-f18537aa8914
- Product NDC
- 70710-1698
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- Venlafaxine Hydrochloride
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230518
- Source listing expiry
- 20271231
Source-listed ingredients
- VENLAFAXINE HYDROCHLORIDE — 37.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-0) · 70710-1698-0
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-3) · 70710-1698-3
- 10 BLISTER PACK in 1 CARTON (70710-1698-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70710-1698-2) · 70710-1698-4
- 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-5) · 70710-1698-5
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-9) · 70710-1698-9
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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