Package 42858-707-03

{"route": ["ORAL"], "spl_id": "e1121b5e-880e-4da8-b4c9-ce8210448c76", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738803", "1738805", "1738807"], "spl_set_id": ["f562ab1a-adb9-4154-81cd-ceb480234331"], "manufacturer_name": ["Rhodes Pharmaceuticals L.P."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-707-03)", "package_ndc": "42858-707-03", "marketing_end_date": "20260731", "marketing_start_date": "20180914"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-707-50)", "package_ndc": "42858-707-50", "marketing_end_date": "20260731", "marketing_start_date": "20180914"}], "brand_name": "PAROXETINE", "product_id": "42858-707_e1121b5e-880e-4da8-b4c9-ce8210448c76", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "42858-707", "generic_name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "labeler_name": "Rhodes Pharmaceuticals L.P.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PAROXETINE", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA209293", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20180914"}