Package 68180-755-01

{"route": ["ORAL"], "spl_id": "53566d4f-ff40-4815-b922-3416cde56fb1", "openfda": {"upc": ["0368180459019"], "unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898342", "898346", "898350", "898353", "898356", "898359"], "spl_set_id": ["968c611b-43a7-40f0-9ed3-aa67ee88364b"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68180-755-01)", "package_ndc": "68180-755-01", "marketing_start_date": "20100205"}], "brand_name": "Amlodipine Besylate and Benazepril Hydrochloride", "product_id": "68180-755_53566d4f-ff40-4815-b922-3416cde56fb1", "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": "68180-755", "generic_name": "Amlodipine Besylate and Benazepril Hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "2.5 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078466", "marketing_category": "ANDA", "marketing_start_date": "20100205", "listing_expiration_date": "20261231"}