Package 83324-109-01

{"route": ["ORAL"], "spl_id": "3806291c-fce8-bcac-e063-6294a90ae162", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["84b9e9a4-b805-420e-83be-ebe98776d1ee"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 PACKAGE (83324-109-01)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "83324-109-01", "marketing_start_date": "20250520"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (83324-109-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "83324-109-50", "marketing_start_date": "20250520"}], "brand_name": "Naproxen Sodium", "product_id": "83324-109_3806291c-fce8-bcac-e063-6294a90ae162", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "83324-109", "generic_name": "NAPROXEN SODIUM", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA079096", "marketing_category": "ANDA", "marketing_start_date": "20250520", "listing_expiration_date": "20261231"}