Package 70518-2652-1

{"route": ["ORAL"], "spl_id": "4a7c93b2-9399-047b-e063-6294a90af72c", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["f56a0f70-bbb1-4e69-b969-965a72f0e2f0"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-2652-0)", "package_ndc": "70518-2652-0", "marketing_start_date": "20200325"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2652-1)", "package_ndc": "70518-2652-1", "marketing_start_date": "20200327"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-2652-2)", "package_ndc": "70518-2652-2", "marketing_start_date": "20201223"}], "brand_name": "venlafaxine", "product_id": "70518-2652_4a7c93b2-9399-047b-e063-6294a90af72c", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-2652", "generic_name": "venlafaxine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20200325", "listing_expiration_date": "20271231"}