Home NDC 70710-1699-2 NDC 70710-1699-2 - Venlafaxine Hydrochloride This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 70710-1699
Requested NDC 70710-1699-2
Package NDCs from labels 70710-1699-5, 70710-1699-0, 70710-1699-2, 70710-1699-4, 70710-1699-3, 70710-1699-9
Manufacturer Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited
Effective date 2026-01-12
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70710-1699-0 Venlafaxine Hydrochloride 1000 in 1 BOTTLE CAPSULE, EXTENDED RELEASE 1000 3 70710-1699-2 Venlafaxine Hydrochloride 10 in 1 BLISTER PACK CAPSULE, EXTENDED RELEASE 10 3 70710-1699-3 Venlafaxine Hydrochloride 30 in 1 BOTTLE CAPSULE, EXTENDED RELEASE 30 3 70710-1699-4 Venlafaxine Hydrochloride 10 in 1 CARTON CAPSULE, EXTENDED RELEASE 10 3 70710-1699-5 Venlafaxine Hydrochloride 500 in 1 BOTTLE CAPSULE, EXTENDED RELEASE 500 3 70710-1699-9 Venlafaxine Hydrochloride 90 in 1 BOTTLE CAPSULE, EXTENDED RELEASE 90 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70710-1699 VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [ZYDUS PHARMACEUTICALS USA INC.] 2 Current NDC, 6 package rows 20230905_9fda0f8d-b24e-4581-9dca-7aaaf86e2413.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 116 of 125 · 2,494 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.