Package 43063-909-30

{"route": ["ORAL"], "spl_id": "302b48e9-e562-b7d7-e063-6394a90a3980", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["c5146d73-2f34-4dfe-ac29-97071279dc4d"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-909-20)", "package_ndc": "43063-909-20", "marketing_start_date": "20210327"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-909-30)", "package_ndc": "43063-909-30", "marketing_start_date": "20210327"}], "brand_name": "Naproxen Sodium", "product_id": "43063-909_302b48e9-e562-b7d7-e063-6394a90a3980", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "43063-909", "generic_name": "Naproxen Sodium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20140411", "listing_expiration_date": "20261231"}