Package 76420-637-01

{"route": ["ORAL"], "spl_id": "07f76fa9-dba3-997b-e063-6294a90a6dd5", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849398", "849431"], "spl_set_id": ["b0571e62-9330-438d-a2ba-873477f52dc4"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-637-01)", "package_ndc": "76420-637-01", "marketing_start_date": "20231018"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-637-30)", "package_ndc": "76420-637-30", "marketing_start_date": "20231018"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-637-60)", "package_ndc": "76420-637-60", "marketing_start_date": "20231018"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-637-90)", "package_ndc": "76420-637-90", "marketing_start_date": "20231018"}], "brand_name": "Naproxen Sodium", "product_id": "76420-637_07f76fa9-dba3-997b-e063-6294a90a6dd5", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "76420-637", "generic_name": "Naproxen Sodium", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "275 mg/1"}], "application_number": "ANDA212199", "marketing_category": "ANDA", "marketing_start_date": "20191030", "listing_expiration_date": "20261231"}