Package 50090-5137-0

{"route": ["ORAL"], "spl_id": "2fd7951a-a945-496b-9c88-93e87eb08fd7", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898342"], "spl_set_id": ["7a75935a-31af-4571-b7d9-8c297a635b57"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-5137-0)", "package_ndc": "50090-5137-0", "marketing_start_date": "20200827"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-5137-1)", "package_ndc": "50090-5137-1", "marketing_start_date": "20200831"}], "brand_name": "Amlodipine Besylate and Benazepril Hydrochloride", "product_id": "50090-5137_2fd7951a-a945-496b-9c88-93e87eb08fd7", "dosage_form": "CAPSULE", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Decreased Blood Pressure [PE]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "50090-5137", "generic_name": "Amlodipine Besylate and Benazepril Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA077183", "marketing_category": "ANDA", "marketing_start_date": "20100419", "listing_expiration_date": "20261231"}