Package 31722-100-31

{"route": ["ORAL"], "spl_id": "4729e7ee-3333-ee2b-e063-6394a90aa85c", "openfda": {"nui": ["N0000175485"], "upc": ["0331722100311"], "unii": ["SOA12P041N"], "rxcui": ["427163"], "spl_set_id": ["295011e1-f919-4e5a-b9e7-4c784f623a86"], "pharm_class_epc": ["Antiprotozoal [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (31722-100-30)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "31722-100-30", "marketing_start_date": "20250415"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (31722-100-31)  / 12 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "31722-100-31", "marketing_start_date": "20250415"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (31722-100-32)  / 6 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "31722-100-32", "marketing_start_date": "20250415"}], "brand_name": "Nitazoxanide", "product_id": "31722-100_4729e7ee-3333-ee2b-e063-6394a90aa85c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antiprotozoal [EPC]"], "product_ndc": "31722-100", "generic_name": "Nitazoxanide", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nitazoxanide", "active_ingredients": [{"name": "NITAZOXANIDE", "strength": "500 mg/1"}], "application_number": "ANDA218701", "marketing_category": "ANDA", "marketing_start_date": "20250415", "listing_expiration_date": "20261231"}