Package 43386-356-10

{"route": ["ORAL"], "spl_id": "2cb73d19-0ef9-4d59-a2de-b7b2b3a369a1", "openfda": {"upc": ["0343386357031", "0343386358014", "0343386356010"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856999", "857002", "857005"], "spl_set_id": ["26a2178e-e0e5-4d61-81fd-e30a3142f1f2"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (43386-356-01)", "package_ndc": "43386-356-01", "marketing_start_date": "20161201"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (43386-356-05)", "package_ndc": "43386-356-05", "marketing_start_date": "20161201"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (43386-356-10)", "package_ndc": "43386-356-10", "marketing_start_date": "20161201"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "43386-356_2cb73d19-0ef9-4d59-a2de-b7b2b3a369a1", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "43386-356", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Lupin Pharmaceuticals,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": "ANDA206245", "marketing_category": "ANDA", "marketing_start_date": "20161201", "listing_expiration_date": "20261231"}