Package 43386-352-05

{"route": ["ORAL"], "spl_id": "cc982f78-de8c-4384-9f43-ffad4169abdd", "openfda": {"upc": ["0343386351039", "0343386352036", "0343386353057"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856980", "856987", "856992"], "spl_set_id": ["48cc1378-ffab-4645-95bb-a05d78066575"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (43386-352-01)", "package_ndc": "43386-352-01", "marketing_start_date": "20161114"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (43386-352-05)", "package_ndc": "43386-352-05", "marketing_start_date": "20161114"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "43386-352_cc982f78-de8c-4384-9f43-ffad4169abdd", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "43386-352", "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": "300 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "7.5 mg/1"}], "application_number": "ANDA206142", "marketing_category": "ANDA", "marketing_start_date": "20161114", "listing_expiration_date": "20261231"}