Package 71930-043-12

{"route": ["ORAL"], "spl_id": "81111908-961b-431d-ac76-379df2ea1406", "openfda": {"upc": ["0371930044120"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856980", "856987", "856992"], "spl_set_id": ["8a201e19-3e47-7e58-e053-2995a90ab1d5"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71930-043-12)", "package_ndc": "71930-043-12", "marketing_start_date": "20190617"}], "brand_name": "hydrocodone bitartrate and acetaminophen", "product_id": "71930-043_81111908-961b-431d-ac76-379df2ea1406", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "71930-043", "dea_schedule": "CII", "generic_name": "hydrocodone bitartrate and acetaminophen", "labeler_name": "Eywa Pharma 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": "ANDA207509", "marketing_category": "ANDA", "marketing_start_date": "20190617", "listing_expiration_date": "20271231"}