Package 67046-1656-3
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
67046-1656-3
Digits Only
6704616563
Product NDC
67046-1656
Description
30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (67046-1656-3)
Marketing
Marketing Status
Brand
venlafaxine hydrochloride
Generic
venlafaxine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a00703b-e5b8-ce3d-e063-6394a90a399e", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581"], "spl_set_id": ["4a007068-89d9-c296-e063-6394a90ad6d0"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (67046-1656-3)", "package_ndc": "67046-1656-3", "marketing_start_date": "20260204"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "67046-1656_4a00703b-e5b8-ce3d-e063-6394a90a399e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "67046-1656", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA217390", "marketing_category": "ANDA", "marketing_start_date": "20260204", "listing_expiration_date": "20271231"}