Package 47682-237-46

{"route": ["ORAL"], "spl_id": "3e4cf134-89dd-0093-e063-6394a90a3c63", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["f6261d45-df1f-483b-b013-3cd6f78d9d43"], "manufacturer_name": ["Unifirst First Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 PACKET in 1 BOX (47682-237-33)  / 1 TABLET, FILM COATED in 1 PACKET (47682-237-46)", "package_ndc": "47682-237-33", "marketing_start_date": "20081230"}, {"sample": false, "description": "1 TABLET, FILM COATED in 1 PACKET (47682-237-46)", "package_ndc": "47682-237-46", "marketing_start_date": "20081230"}, {"sample": false, "description": "50 PACKET in 1 BOX (47682-237-50)  / 1 TABLET, FILM COATED in 1 PACKET", "package_ndc": "47682-237-50", "marketing_start_date": "20081230"}], "brand_name": "Medique Mediproxen", "product_id": "47682-237_3e4cf134-89dd-0093-e063-6394a90a3c63", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "47682-237", "generic_name": "NAPROXEN SODIUM", "labeler_name": "Unifirst First Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Medique Mediproxen", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA079096", "marketing_category": "ANDA", "marketing_start_date": "20081230", "listing_expiration_date": "20261231"}