Package 68071-2198-9

{"route": ["ORAL"], "spl_id": "1d75dc5e-3f66-d0c3-e063-6294a90aac2b", "openfda": {"upc": ["0368071219890"], "unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["4f45c818-b324-6ca6-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-2198-3)", "package_ndc": "68071-2198-3", "marketing_start_date": "20170511"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-2198-6)", "package_ndc": "68071-2198-6", "marketing_start_date": "20170511"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-2198-9)", "package_ndc": "68071-2198-9", "marketing_start_date": "20170511"}], "brand_name": "Citalopram Hydrobromide", "product_id": "68071-2198_1d75dc5e-3f66-d0c3-e063-6294a90aac2b", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-2198", "generic_name": "Citalopram Hydrobromide", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20261231"}