Package 64850-632-01

{"route": ["ORAL"], "spl_id": "91acad07-a9ce-450e-b9f6-4401b89bd32c", "openfda": {"upc": ["0364850630016", "0364850633017", "0364850632010", "0364850631013"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856999", "857002", "857005", "857391"], "spl_set_id": ["89b8145f-5310-4b58-a65d-586dc90d642d"], "manufacturer_name": ["Elite Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (64850-632-01)", "package_ndc": "64850-632-01", "marketing_start_date": "20181116"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "64850-632_91acad07-a9ce-450e-b9f6-4401b89bd32c", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "64850-632", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Elite Laboratories, 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": "ANDA209924", "marketing_category": "ANDA", "marketing_start_date": "20181116", "listing_expiration_date": "20261231"}