Package 60687-915-01

{"route": ["ORAL"], "spl_id": "47e2f52f-946b-05e5-e063-6294a90a5a59", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563", "1099569"], "spl_set_id": ["b12b76a0-4b6e-4cd4-9508-10a2c84d8beb"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-915-01)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-915-11)", "package_ndc": "60687-915-01", "marketing_start_date": "20251229"}, {"sample": false, "description": "80 BLISTER PACK in 1 CARTON (60687-915-02)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-915-93)", "package_ndc": "60687-915-02", "marketing_start_date": "20260108"}], "brand_name": "divalproex sodium", "product_id": "60687-915_47e2f52f-946b-05e5-e063-6294a90a5a59", "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": "60687-915", "generic_name": "divalproex sodium", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA214643", "marketing_category": "ANDA", "marketing_start_date": "20251229", "listing_expiration_date": "20271231"}