Package 13107-213-99

{"route": ["ORAL"], "spl_id": "265ff2e7-c060-4a82-909b-26e71c262dd6", "openfda": {"upc": ["0313107213014", "0313107211010"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856980", "856987", "856992"], "spl_set_id": ["392a846e-7325-462d-b19b-8afda44c5cb0"], "manufacturer_name": ["Aurolife Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13107-213-01)", "package_ndc": "13107-213-01", "marketing_start_date": "20150506"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (13107-213-05)", "package_ndc": "13107-213-05", "marketing_start_date": "20150506"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (13107-213-30)", "package_ndc": "13107-213-30", "marketing_start_date": "20150506"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (13107-213-99)", "package_ndc": "13107-213-99", "marketing_start_date": "20150506"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "13107-213_265ff2e7-c060-4a82-909b-26e71c262dd6", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "13107-213", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Aurolife Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA207709", "marketing_category": "ANDA", "marketing_start_date": "20150506", "listing_expiration_date": "20261231"}