Package 51655-939-55

{"route": ["ORAL"], "spl_id": "497450db-876a-701a-e063-6394a90a62ae", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198148"], "spl_set_id": ["f77f4a5a-b307-84ff-e053-6294a90aba5b"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET in 1 BOTTLE, PLASTIC (51655-939-07)", "package_ndc": "51655-939-07", "marketing_start_date": "20220927"}, {"sample": false, "description": "5 TABLET in 1 BOTTLE, PLASTIC (51655-939-55)", "package_ndc": "51655-939-55", "marketing_start_date": "20220804"}], "brand_name": "PredniSONE", "product_id": "51655-939_497450db-876a-701a-e063-6394a90a62ae", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51655-939", "generic_name": "PredniSONE", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PredniSONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "50 mg/1"}], "application_number": "ANDA084283", "marketing_category": "ANDA", "marketing_start_date": "20220804", "listing_expiration_date": "20271231"}