Package 76420-215-01

{"route": ["ORAL"], "spl_id": "dea38bcd-012c-0949-e053-2a95a90a8f7b", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856999"], "spl_set_id": ["5c00f98f-dcab-4bdb-901e-02eb873dea31"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-215-01)", "package_ndc": "76420-215-01", "marketing_start_date": "20220510"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-215-30)", "package_ndc": "76420-215-30", "marketing_start_date": "20220510"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-215-60)", "package_ndc": "76420-215-60", "marketing_start_date": "20220510"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-215-90)", "package_ndc": "76420-215-90", "marketing_start_date": "20220510"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "76420-215_dea38bcd-012c-0949-e053-2a95a90a8f7b", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "76420-215", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA202991", "marketing_category": "ANDA", "marketing_start_date": "20160412", "listing_expiration_date": "20261231"}