lisinopril and hydrochlorothiazide (70518-3505)

Drug Facts

Product Profile

Brand Name lisinopril and hydrochlorothiazide

Generic Name lisinopril and hydrochlorothiazide tablets

Labeler remedyrepack inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 12.5 mg/1, lisinopril 20 mg/1

Manufacturer

REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3505

Product ID 70518-3505_43cf84c0-fbc9-c75c-e063-6394a90ac53f

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA076230

Listing Expiration 2026-12-31

Marketing Start 2022-08-31

Pharmacologic Class

Established (EPC)

thiazide diuretic [epc]

Chemical Structure

thiazides [cs]

Physiologic Effect

increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183505

Hyphenated Format 70518-3505

Supplemental Identifiers

RxCUI

197886

UNII

0J48LPH2TH E7199S1YWR

NUI

N0000175359 N0000175419 M0471776

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lisinopril and hydrochlorothiazide (source: ndc)

Generic Name lisinopril and hydrochlorothiazide tablets (source: ndc)

Application Number ANDA076230 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

12.5 mg/1
20 mg/1

source: ndc

Packaging

90 TABLET in 1 BOTTLE, PLASTIC (70518-3505-0)
30 TABLET in 1 BLISTER PACK (70518-3505-1)
100 TABLET in 1 BOTTLE, PLASTIC (70518-3505-4)

source: ndc

Packages (3)

70518-3505-0 90 TABLET in 1 BOTTLE, PLASTIC (70518-3505-0) 70518-3505-1 30 TABLET in 1 BLISTER PACK (70518-3505-1) 70518-3505-4 100 TABLET in 1 BOTTLE, PLASTIC (70518-3505-4)

Ingredients (2)

hydrochlorothiazide (12.5 mg/1) lisinopril (20 mg/1)

Linked Drug Pages (1)

Lisinopril and Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "43cf84c0-fbc9-c75c-e063-6394a90ac53f", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197886"], "spl_set_id": ["3bea11a3-eb07-46b2-9b91-f8a48a2f3b7e"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3505-0)", "package_ndc": "70518-3505-0", "marketing_start_date": "20220831"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3505-1)", "package_ndc": "70518-3505-1", "marketing_start_date": "20220922"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-3505-4)", "package_ndc": "70518-3505-4", "marketing_start_date": "20250320"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "70518-3505_43cf84c0-fbc9-c75c-e063-6394a90ac53f", "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": "70518-3505", "generic_name": "Lisinopril and Hydrochlorothiazide Tablets", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA076230", "marketing_category": "ANDA", "marketing_start_date": "20220831", "listing_expiration_date": "20261231"}