Package 71335-2091-6

Brand: lisinopril and hydrochlorothiazide

Generic: lisinopril and hydrochlorothiazide tablets
NDC Package

Package Facts

Identity

Package NDC 71335-2091-6
Digits Only 7133520916
Product NDC 71335-2091
Description

180 TABLET in 1 BOTTLE (71335-2091-6)

Marketing

Marketing Status
Marketed Since 2022-05-17
Brand lisinopril and hydrochlorothiazide
Generic lisinopril and hydrochlorothiazide tablets
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "746b1295-24a9-46f9-9032-2d85c0367205", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197887"], "spl_set_id": ["5885b1ff-715c-4f90-b43d-bddf94d61acd"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2091-1)", "package_ndc": "71335-2091-1", "marketing_start_date": "20220517"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2091-2)", "package_ndc": "71335-2091-2", "marketing_start_date": "20220517"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2091-3)", "package_ndc": "71335-2091-3", "marketing_start_date": "20220517"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2091-4)", "package_ndc": "71335-2091-4", "marketing_start_date": "20220517"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2091-5)", "package_ndc": "71335-2091-5", "marketing_start_date": "20220517"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-2091-6)", "package_ndc": "71335-2091-6", "marketing_start_date": "20220517"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "71335-2091_746b1295-24a9-46f9-9032-2d85c0367205", "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": "71335-2091", "generic_name": "Lisinopril and Hydrochlorothiazide Tablets", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA076230", "marketing_category": "ANDA", "marketing_start_date": "20150312", "listing_expiration_date": "20261231"}