Package 70518-2259-1

{"route": ["ORAL"], "spl_id": "49ef8066-9ca5-1d82-e063-6394a90a74a5", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581"], "spl_set_id": ["50d3b487-9f65-4e2f-b6eb-9533964f8972"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2259-1)", "package_ndc": "70518-2259-1", "marketing_start_date": "20200819"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-2259-2)", "package_ndc": "70518-2259-2", "marketing_start_date": "20201102"}, {"sample": false, "description": "30 POUCH in 1 BOX (70518-2259-5)  / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-2259-6)", "package_ndc": "70518-2259-5", "marketing_start_date": "20230828"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "70518-2259_49ef8066-9ca5-1d82-e063-6394a90a74a5", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-2259", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20190809", "listing_expiration_date": "20271231"}