Package 0245-0411-11

{"route": ["ORAL"], "spl_id": "39e7eaec-9677-7a63-e063-6394a90a520e", "openfda": {"unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856999", "857002", "857005"], "spl_set_id": ["3aa0b733-b58f-46bd-8e76-37ddf1dc3356"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0245-0411-01)  / 1 TABLET in 1 BLISTER PACK (0245-0411-89)", "package_ndc": "0245-0411-01", "marketing_start_date": "20170327"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (0245-0411-11)", "package_ndc": "0245-0411-11", "marketing_start_date": "20170327"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0245-0411-50)", "package_ndc": "0245-0411-50", "marketing_start_date": "20170327"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "0245-0411_39e7eaec-9677-7a63-e063-6394a90a520e", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "0245-0411", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Upsher-Smith Laboratories, LLC", "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": "ANDA206484", "marketing_category": "ANDA", "marketing_start_date": "20170327", "listing_expiration_date": "20261231"}