Package 0406-0378-62

{"route": ["ORAL"], "spl_id": "1c335808-6b36-42f1-b811-284ac384d01a", "openfda": {"upc": ["0304060377059", "0304060376052", "0304060378056"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856980", "856987", "856992"], "spl_set_id": ["d621b526-4d9a-48a9-9a3e-d29d6aea2f31"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0406-0378-01)", "package_ndc": "0406-0378-01", "marketing_start_date": "20170331"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0406-0378-05)", "package_ndc": "0406-0378-05", "marketing_start_date": "20170331"}, {"sample": false, "description": "1 TABLET in 1 BLISTER PACK (0406-0378-23)", "package_ndc": "0406-0378-23", "marketing_start_date": "20170331"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (0406-0378-62)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "0406-0378-62", "marketing_start_date": "20170331"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "0406-0378_1c335808-6b36-42f1-b811-284ac384d01a", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "0406-0378", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "SpecGx 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": "ANDA206718", "marketing_category": "ANDA", "marketing_start_date": "20170331", "listing_expiration_date": "20261231"}