Package 25000-609-03

{"route": ["ORAL"], "spl_id": "c8aa863f-eb1f-4b66-9ec6-2af2c7958248", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["3686cde5-f76d-4d16-aa5d-caceb8408f8c"], "manufacturer_name": ["MARKSANS PHARMA LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-609-03)", "package_ndc": "25000-609-03", "marketing_start_date": "20220527"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-609-07)", "package_ndc": "25000-609-07", "marketing_start_date": "20220527"}], "brand_name": "Duloxetine", "product_id": "25000-609_c8aa863f-eb1f-4b66-9ec6-2af2c7958248", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "25000-609", "generic_name": "Duloxetine Hydrochloride", "labeler_name": "MARKSANS PHARMA LIMITED", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090723", "marketing_category": "ANDA", "marketing_start_date": "20220527", "listing_expiration_date": "20261231"}