Package 50844-471-11

{"route": ["ORAL"], "spl_id": "831bfaae-6043-4bb8-9ca2-0ec4043040a7", "openfda": {"upc": ["0350844471161"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["6161b881-f422-47ae-86ba-a28d669bce79"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 POUCH in 1 CARTON (50844-471-11)  / 1 TABLET, FILM COATED in 1 POUCH (50844-471-43)", "package_ndc": "50844-471-11", "marketing_start_date": "20200916"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-14)", "package_ndc": "50844-471-14", "marketing_start_date": "20200916"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-16)", "package_ndc": "50844-471-16", "marketing_start_date": "20200916"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-471-19)  / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-471-19", "marketing_start_date": "20200916"}, {"sample": false, "description": "48 POUCH in 1 CARTON (50844-471-22)  / 1 TABLET, FILM COATED in 1 POUCH (50844-471-43)", "package_ndc": "50844-471-22", "marketing_start_date": "20200916"}, {"sample": false, "description": "25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-56)", "package_ndc": "50844-471-56", "marketing_start_date": "20200916"}, {"sample": false, "description": "8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-98)", "package_ndc": "50844-471-98", "marketing_start_date": "20200916"}, {"sample": false, "description": "8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-99)", "package_ndc": "50844-471-99", "marketing_start_date": "20200916"}], "brand_name": "Naproxen Headache Pain", "product_id": "50844-471_831bfaae-6043-4bb8-9ca2-0ec4043040a7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50844-471", "generic_name": "Naproxen Sodium", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Headache Pain", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20200916", "listing_expiration_date": "20261231"}