Package 76420-257-90

{"route": ["ORAL"], "spl_id": "e436e361-d992-7d6d-e053-2995a90a10e4", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857005"], "spl_set_id": ["23dde6b8-3655-49ee-ac2c-28f80cf6b3c2"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-257-30)", "package_ndc": "76420-257-30", "marketing_start_date": "20220720"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-257-60)", "package_ndc": "76420-257-60", "marketing_start_date": "20220720"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-257-90)", "package_ndc": "76420-257-90", "marketing_start_date": "20220720"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "76420-257_e436e361-d992-7d6d-e053-2995a90a10e4", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "76420-257", "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": "7.5 mg/1"}], "application_number": "ANDA202991", "marketing_category": "ANDA", "marketing_start_date": "20160412", "listing_expiration_date": "20261231"}