Package 65862-043-30
Brand: lisinopril and hydrochlorothiazide
Generic: lisinopril and hydrochlorothiazidePackage Facts
Identity
Package NDC
65862-043-30
Digits Only
6586204330
Product NDC
65862-043
Description
30 TABLET in 1 BOTTLE (65862-043-30)
Marketing
Marketing Status
Brand
lisinopril and hydrochlorothiazide
Generic
lisinopril and hydrochlorothiazide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5e2383b2-8c0d-450f-b681-74bfb12942a7", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197885", "197886", "197887"], "spl_set_id": ["d7214539-6c3d-466a-a474-6fde096fa182"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-043-00)", "package_ndc": "65862-043-00", "marketing_start_date": "20060314"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-043-01)", "package_ndc": "65862-043-01", "marketing_start_date": "20060314"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65862-043-05)", "package_ndc": "65862-043-05", "marketing_start_date": "20060314"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (65862-043-30)", "package_ndc": "65862-043-30", "marketing_start_date": "20060314"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65862-043-99)", "package_ndc": "65862-043-99", "marketing_start_date": "20060314"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "65862-043_5e2383b2-8c0d-450f-b681-74bfb12942a7", "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": "65862-043", "generic_name": "Lisinopril and Hydrochlorothiazide", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LISINOPRIL", "strength": "10 mg/1"}], "application_number": "ANDA077606", "marketing_category": "ANDA", "marketing_start_date": "20060314", "listing_expiration_date": "20261231"}