Package 51655-213-26

{"route": ["ORAL"], "spl_id": "48d2a75b-7672-5a6d-e063-6294a90a18b8", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898342"], "spl_set_id": ["f2b56630-4e3a-6f9c-e053-2a95a90a4650"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (51655-213-26)", "package_ndc": "51655-213-26", "marketing_start_date": "20221020"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (51655-213-52)", "package_ndc": "51655-213-52", "marketing_start_date": "20230502"}], "brand_name": "Amlodipine and Benazepril Hydrochloride", "product_id": "51655-213_48d2a75b-7672-5a6d-e063-6294a90a18b8", "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": "51655-213", "generic_name": "Amlodipine and Benazepril Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA202239", "marketing_category": "ANDA", "marketing_start_date": "20221020", "listing_expiration_date": "20271231"}