Package 49483-608-00

{"route": ["ORAL"], "spl_id": "0538c5c7-c559-4ea9-e063-6294a90aec21", "openfda": {"upc": ["0349483608014", "0349483608311"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["ab7b7b8e-923b-4dc1-812c-78e85de1bee1"], "manufacturer_name": ["TIME CAP LABORATORIES, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6500 TABLET, FILM COATED in 1 BAG (49483-608-00)", "package_ndc": "49483-608-00", "marketing_start_date": "20160328"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (49483-608-01)", "package_ndc": "49483-608-01", "marketing_start_date": "20160328"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (49483-608-05)", "package_ndc": "49483-608-05", "marketing_start_date": "20160328"}, {"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE (49483-608-31)", "package_ndc": "49483-608-31", "marketing_start_date": "20230808"}], "brand_name": "NAPROXEN SODIUM", "product_id": "49483-608_0538c5c7-c559-4ea9-e063-6294a90aec21", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "49483-608", "generic_name": "NAPROXEN SODIUM", "labeler_name": "TIME CAP LABORATORIES, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NAPROXEN SODIUM", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA090545", "marketing_category": "ANDA", "marketing_start_date": "20160328", "listing_expiration_date": "20261231"}