Package 10702-055-01

{"route": ["ORAL"], "spl_id": "47ba86ad-2410-e733-e063-6394a90a24e3", "openfda": {"unii": ["68JRS2HC1C", "NO70W886KK"], "rxcui": ["992656"], "spl_set_id": ["26d7c90c-5e6b-4bdb-b06f-c76173a01c21"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-055-01)", "package_ndc": "10702-055-01", "marketing_start_date": "20170807"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (10702-055-03)", "package_ndc": "10702-055-03", "marketing_start_date": "20170807"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (10702-055-09)", "package_ndc": "10702-055-09", "marketing_start_date": "20170807"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (10702-055-10)", "package_ndc": "10702-055-10", "marketing_start_date": "20170807"}], "brand_name": "Hydrocodone Bitartrate and Homatropine Methylbromide", "product_id": "10702-055_47ba86ad-2410-e733-e063-6394a90a24e3", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "10702-055", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Homatropine Methylbromide", "labeler_name": "KVK-Tech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Homatropine Methylbromide", "active_ingredients": [{"name": "HOMATROPINE METHYLBROMIDE", "strength": "1.5 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "5 mg/1"}], "application_number": "ANDA207176", "marketing_category": "ANDA", "marketing_start_date": "20170807", "listing_expiration_date": "20271231"}