Package 65862-155-90

{"route": ["ORAL"], "spl_id": "19f7a08f-58bd-45b8-a750-4432ae161455", "openfda": {"upc": ["0365862154019"], "unii": ["X2ELS050D8"], "rxcui": ["1738483", "1738495", "1738503", "1738511"], "spl_set_id": ["326e8ab0-6886-4749-9544-885b37070051"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-155-01)", "package_ndc": "65862-155-01", "marketing_start_date": "20070725"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-155-05)", "package_ndc": "65862-155-05", "marketing_start_date": "20070725"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-155-30)", "package_ndc": "65862-155-30", "marketing_start_date": "20070725"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-155-90)", "package_ndc": "65862-155-90", "marketing_start_date": "20070725"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-155-99)", "package_ndc": "65862-155-99", "marketing_start_date": "20070725"}], "brand_name": "Paroxetine", "product_id": "65862-155_19f7a08f-58bd-45b8-a750-4432ae161455", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65862-155", "generic_name": "Paroxetine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA078406", "marketing_category": "ANDA", "marketing_start_date": "20070725", "listing_expiration_date": "20261231"}