Package 46708-793-31

{"route": ["ORAL"], "spl_id": "e3e238db-4388-49bb-aa67-6d73adbb2280", "openfda": {"upc": ["0346708794309"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["e3e238db-4388-49bb-aa67-6d73adbb2280"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-793-30)", "package_ndc": "46708-793-30", "marketing_start_date": "20240610"}, {"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-793-31)", "package_ndc": "46708-793-31", "marketing_start_date": "20240610"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-793-71)", "package_ndc": "46708-793-71", "marketing_start_date": "20240610"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-793-90)", "package_ndc": "46708-793-90", "marketing_start_date": "20240610"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-793-91)", "package_ndc": "46708-793-91", "marketing_start_date": "20240610"}], "brand_name": "VENLAFAXINE HYDROCHLORIDE", "product_id": "46708-793_e3e238db-4388-49bb-aa67-6d73adbb2280", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "46708-793", "generic_name": "VENLAFAXINE HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENLAFAXINE HYDROCHLORIDE", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA217767", "marketing_category": "ANDA", "marketing_start_date": "20240610", "listing_expiration_date": "20261231"}