Package 50090-3136-2

{"route": ["ORAL"], "spl_id": "327ed657-6e36-4573-87ca-65064e46db9f", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["c6730edc-7226-4521-a04a-1bf296b01b8d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-3136-0)", "package_ndc": "50090-3136-0", "marketing_start_date": "20170913"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-3136-1)", "package_ndc": "50090-3136-1", "marketing_start_date": "20240212"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-3136-2)", "package_ndc": "50090-3136-2", "marketing_start_date": "20180822"}], "brand_name": "Citalopram", "product_id": "50090-3136_327ed657-6e36-4573-87ca-65064e46db9f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-3136", "generic_name": "Citalopram Hydrobromide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077031", "marketing_category": "ANDA", "marketing_start_date": "20041028", "listing_expiration_date": "20261231"}