Package 50090-6770-0

{"route": ["ORAL"], "spl_id": "2d7c6212-c292-4857-8baa-d2bb485b6fa9", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898353"], "spl_set_id": ["89d8d490-3a9c-40f2-86b7-94b5101dd09a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-6770-0)", "package_ndc": "50090-6770-0", "marketing_start_date": "20231023"}], "brand_name": "Amlodipine and Benazepril Hydrochloride", "product_id": "50090-6770_2d7c6212-c292-4857-8baa-d2bb485b6fa9", "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": "50090-6770", "generic_name": "Amlodipine and Benazepril Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202239", "marketing_category": "ANDA", "marketing_start_date": "20120905", "listing_expiration_date": "20261231"}