Package 51655-310-53

{"route": ["ORAL"], "spl_id": "48eae225-e9e6-201c-e063-6294a90a67b2", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["f2b920b2-f8b3-1e6e-e053-2a95a90ae153"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (51655-310-53)", "package_ndc": "51655-310-53", "marketing_start_date": "20221128"}], "brand_name": "Furosemide", "product_id": "51655-310_48eae225-e9e6-201c-e063-6294a90a67b2", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "51655-310", "generic_name": "furosemide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20221128", "listing_expiration_date": "20271231"}