Package 70518-2107-3

{"route": ["ORAL"], "spl_id": "499ef330-088a-7248-e063-6394a90af248", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["ac9b972d-8b8a-4727-90c2-b208f91272fd"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-2107-3)  / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-2107-4)", "package_ndc": "70518-2107-3", "marketing_start_date": "20230826"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-2107-5)", "package_ndc": "70518-2107-5", "marketing_start_date": "20250731"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "70518-2107_499ef330-088a-7248-e063-6394a90af248", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-2107", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20190523", "listing_expiration_date": "20271231"}