Package 71335-2535-3

{"route": ["ORAL"], "spl_id": "41db30e4-4563-57fd-e063-6294a90a4cfe", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["d524db34-99c4-4837-a532-a619f82c21ba"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2535-1)", "package_ndc": "71335-2535-1", "marketing_start_date": "20241210"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2535-2)", "package_ndc": "71335-2535-2", "marketing_start_date": "20241210"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2535-3)", "package_ndc": "71335-2535-3", "marketing_start_date": "20241210"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2535-4)", "package_ndc": "71335-2535-4", "marketing_start_date": "20241210"}], "brand_name": "Divalproex sodium", "product_id": "71335-2535_41db30e4-4563-57fd-e063-6294a90a4cfe", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "71335-2535", "generic_name": "Divalproex sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA215527", "marketing_category": "ANDA", "marketing_start_date": "20230926", "listing_expiration_date": "20261231"}