Package 68084-415-02

{"route": ["ORAL"], "spl_id": "46405f96-5e81-a0c9-e063-6394a90a9592", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563", "1099569"], "spl_set_id": ["a8ba3986-1ded-44a8-8d10-d0f252a07794"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-415-01)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-415-11)", "package_ndc": "68084-415-01", "marketing_end_date": "20261130", "marketing_start_date": "20131121"}, {"sample": false, "description": "80 BLISTER PACK in 1 CARTON (68084-415-02)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-415-93)", "package_ndc": "68084-415-02", "marketing_end_date": "20260630", "marketing_start_date": "20230206"}], "brand_name": "Divalproex Sodium", "product_id": "68084-415_46405f96-5e81-a0c9-e063-6394a90a9592", "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": "68084-415", "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": "ANDA078239", "marketing_category": "ANDA", "marketing_end_date": "20261130", "marketing_start_date": "20131121"}