Package 76420-209-60

{"route": ["ORAL"], "spl_id": "de3d43dc-ba4c-e233-e053-2995a90ac632", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049214"], "spl_set_id": ["3e89f02d-b6e7-4641-82d4-f756518a8914"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (76420-209-01)", "package_ndc": "76420-209-01", "marketing_start_date": "20220505"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (76420-209-30)", "package_ndc": "76420-209-30", "marketing_start_date": "20220505"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (76420-209-60)", "package_ndc": "76420-209-60", "marketing_start_date": "20220505"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (76420-209-90)", "package_ndc": "76420-209-90", "marketing_start_date": "20220505"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "76420-209_de3d43dc-ba4c-e233-e053-2995a90ac632", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "76420-209", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA201278", "marketing_category": "ANDA", "marketing_start_date": "20140828", "listing_expiration_date": "20261231"}