Package 71335-2158-5

{"route": ["ORAL"], "spl_id": "5079c7a7-f979-4b2e-a516-be3c8a9edc03", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099870"], "spl_set_id": ["fbaff0ae-431e-4e83-81c2-41eb4b18ee87"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-1)", "package_ndc": "71335-2158-1", "marketing_start_date": "20220811"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-2)", "package_ndc": "71335-2158-2", "marketing_start_date": "20230302"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-3)", "package_ndc": "71335-2158-3", "marketing_start_date": "20220811"}, {"sample": false, "description": "180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-4)", "package_ndc": "71335-2158-4", "marketing_start_date": "20240906"}, {"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-5)", "package_ndc": "71335-2158-5", "marketing_start_date": "20220920"}], "brand_name": "Divalproex Sodium", "product_id": "71335-2158_5079c7a7-f979-4b2e-a516-be3c8a9edc03", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "71335-2158", "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": "ANDA090554", "marketing_category": "ANDA", "marketing_start_date": "20141024", "listing_expiration_date": "20261231"}