Package 55758-048-50

{"route": ["ORAL"], "spl_id": "2d5725c3-b1fc-ac59-e063-6294a90a3f6e", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["c94c4b6e-a48b-cee5-e053-2995a90a49ac"], "manufacturer_name": ["Pharmadel LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, COATED in 1 PACKET (55758-048-02)", "package_ndc": "55758-048-02", "marketing_start_date": "20231024"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (55758-048-24)  / 24 TABLET, COATED in 1 BOTTLE", "package_ndc": "55758-048-24", "marketing_start_date": "20191009"}, {"sample": false, "description": "25 PACKET in 1 CARTON (55758-048-50)  / 2 TABLET, COATED in 1 PACKET (55758-048-02)", "package_ndc": "55758-048-50", "marketing_start_date": "20231024"}], "brand_name": "Rapidol Naproxen", "product_id": "55758-048_2d5725c3-b1fc-ac59-e063-6294a90a3f6e", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "55758-048", "generic_name": "Naproxen sodium", "labeler_name": "Pharmadel LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Rapidol Naproxen", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA091353", "marketing_category": "ANDA", "marketing_start_date": "20191009", "listing_expiration_date": "20261231"}