Package 43386-710-05

{"route": ["ORAL"], "spl_id": "916f3e69-0d6e-4524-8abe-afb2e134eec2", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "33067B3N2M"], "rxcui": ["310796", "310797", "310809"], "spl_set_id": ["383ecaa6-29c8-4280-a442-c47f101d7c88"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (43386-710-05)", "package_ndc": "43386-710-05", "marketing_start_date": "20110715"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (43386-710-09)", "package_ndc": "43386-710-09", "marketing_start_date": "20110715"}], "brand_name": "Quinapril HCL and Hydrochlorothiazide", "product_id": "43386-710_916f3e69-0d6e-4524-8abe-afb2e134eec2", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "43386-710", "generic_name": "Quinapril HCl and Hydrochlorothiazide", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril HCL and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "QUINAPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076374", "marketing_category": "ANDA", "marketing_start_date": "20110715", "listing_expiration_date": "20261231"}