Package 50090-7677-0

{"route": ["ORAL"], "spl_id": "68698c51-6c2c-425e-a681-fbb382d79968", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858810"], "spl_set_id": ["fd0a7ecc-d6a2-4e04-a14f-1ed4dacb7df3"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7677-0)", "package_ndc": "50090-7677-0", "marketing_start_date": "20251008"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-7677-1)", "package_ndc": "50090-7677-1", "marketing_start_date": "20251008"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7677-3)", "package_ndc": "50090-7677-3", "marketing_start_date": "20251008"}], "brand_name": "ENALAPRIL MALEATE", "product_id": "50090-7677_68698c51-6c2c-425e-a681-fbb382d79968", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "50090-7677", "generic_name": "ENALAPRIL MALEATE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ENALAPRIL MALEATE", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "20 mg/1"}], "application_number": "ANDA075178", "marketing_category": "ANDA", "marketing_start_date": "20250212", "listing_expiration_date": "20261231"}