Package 76420-133-90

{"route": ["ORAL"], "spl_id": "43413993-4070-bd37-e063-6294a90ac4a1", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857002"], "spl_set_id": ["d1de0f93-1439-4ee3-b692-56e1a1400682"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-133-01)", "package_ndc": "76420-133-01", "marketing_start_date": "20251110"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (76420-133-05)", "package_ndc": "76420-133-05", "marketing_start_date": "20251110"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-133-30)", "package_ndc": "76420-133-30", "marketing_start_date": "20201216"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-133-60)", "package_ndc": "76420-133-60", "marketing_start_date": "20251110"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-133-90)", "package_ndc": "76420-133-90", "marketing_start_date": "20251110"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "76420-133_43413993-4070-bd37-e063-6294a90ac4a1", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "76420-133", "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": "5 mg/1"}], "application_number": "ANDA202991", "marketing_category": "ANDA", "marketing_start_date": "20160412", "listing_expiration_date": "20261231"}