Package 68001-474-00

{"route": ["ORAL"], "spl_id": "4b029245-2b01-8812-e063-6394a90afff8", "openfda": {"upc": ["0368001474009", "0368001473002", "0368001472005"], "unii": ["644VL95AO6"], "rxcui": ["1099625", "1099678", "1099870"], "spl_set_id": ["b95494e2-ee7a-7415-e053-2995a90ae852"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-474-00)", "package_ndc": "68001-474-00", "marketing_start_date": "20210120"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-474-03)", "package_ndc": "68001-474-03", "marketing_start_date": "20210120"}], "brand_name": "Divalproex Sodium", "product_id": "68001-474_4b029245-2b01-8812-e063-6394a90afff8", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "68001-474", "generic_name": "Divalproex Sodium", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA079163", "marketing_category": "ANDA", "marketing_start_date": "20210120", "listing_expiration_date": "20271231"}