lisinopril and hydrochlorothiazide

Generic: lisinopril and hydrochlorothiazide

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril and hydrochlorothiazide
Generic Name lisinopril and hydrochlorothiazide
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 12.5 mg/1, lisinopril 20 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4435
Product ID 68071-4435_1a8c4db5-140d-1e19-e063-6294a90ae99c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076194
Listing Expiration 2026-12-31
Marketing Start 2003-03-04

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 680714435
Hyphenated Format 68071-4435

Supplemental Identifiers

RxCUI
197886
UPC
0368071443530
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 (source: ndc)
Application Number ANDA076194 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-4435-3)
  • 60 TABLET in 1 BOTTLE (68071-4435-6)
  • 90 TABLET in 1 BOTTLE (68071-4435-9)
source: ndc

Packages (3)

68071-4435-3 30 TABLET in 1 BOTTLE (68071-4435-3) 68071-4435-6 60 TABLET in 1 BOTTLE (68071-4435-6) 68071-4435-9 90 TABLET in 1 BOTTLE (68071-4435-9)

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": "1a8c4db5-140d-1e19-e063-6294a90ae99c", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368071443530"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197886"], "spl_set_id": ["6c57bf12-9ad5-3a25-e053-2a91aa0aaf26"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-4435-3)", "package_ndc": "68071-4435-3", "marketing_start_date": "20180516"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-4435-6)", "package_ndc": "68071-4435-6", "marketing_start_date": "20180516"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-4435-9)", "package_ndc": "68071-4435-9", "marketing_start_date": "20180516"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "68071-4435_1a8c4db5-140d-1e19-e063-6294a90ae99c", "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": "68071-4435", "generic_name": "Lisinopril and Hydrochlorothiazide", "labeler_name": "NuCare Pharmaceuticals,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": "ANDA076194", "marketing_category": "ANDA", "marketing_start_date": "20030304", "listing_expiration_date": "20261231"}