Package 70771-1651-1

{"route": ["ORAL"], "spl_id": "0bf02fa2-e5cd-42d6-ab41-1ecd150b7c57", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808751", "808753"], "spl_set_id": ["750333ce-a512-42e1-b9e3-179714b488df"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1651-1)", "package_ndc": "70771-1651-1", "marketing_start_date": "20220901"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1651-3)", "package_ndc": "70771-1651-3", "marketing_start_date": "20220901"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1651-9)", "package_ndc": "70771-1651-9", "marketing_start_date": "20220901"}], "brand_name": "Venlafaxine", "product_id": "70771-1651_0bf02fa2-e5cd-42d6-ab41-1ecd150b7c57", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70771-1651", "generic_name": "Venlafaxine", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA215622", "marketing_category": "ANDA", "marketing_start_date": "20220901", "listing_expiration_date": "20261231"}