quinapril and hydrochlorothiazide 20/12.5

Generic: quinapril and hydrochlorothiazide 20/12.5

Labeler: cipla usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quinapril and hydrochlorothiazide 20/12.5
Generic Name quinapril and hydrochlorothiazide 20/12.5
Labeler cipla usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 12.5 mg/1, quinapril hydrochloride 20 mg/1

Manufacturer
Cipla USA Inc.

Identifiers & Regulatory

Product NDC 69097-829
Product ID 69097-829_4d3f7e7a-ed61-4df6-bc45-f38fb4117406
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201356
Listing Expiration 2026-12-31
Marketing Start 2016-07-20

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 69097829
Hyphenated Format 69097-829

Supplemental Identifiers

RxCUI
310796 310797 310809
UPC
0369097831059 0369097829056
UNII
0J48LPH2TH 33067B3N2M
NUI
N0000175359 N0000175419 M0471776

Packaging Origin

Original Packager
true

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 quinapril and hydrochlorothiazide 20/12.5 (source: ndc)
Generic Name quinapril and hydrochlorothiazide 20/12.5 (source: ndc)
Application Number ANDA201356 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (69097-829-05)
source: ndc

Packages (1)

69097-829-05 90 TABLET in 1 BOTTLE (69097-829-05)

Ingredients (2)

hydrochlorothiazide (12.5 mg/1) quinapril hydrochloride (20 mg/1)

Linked Drug Pages (1)

Quinapril and Hydrochlorothiazide 10/12.5, Quinapril and Hydrochlorothiazide 20/12.5, Quinapril and Hydrochlorothiazide 20/25 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4d3f7e7a-ed61-4df6-bc45-f38fb4117406", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0369097831059", "0369097829056"], "unii": ["0J48LPH2TH", "33067B3N2M"], "rxcui": ["310796", "310797", "310809"], "spl_set_id": ["1de5420c-23d6-40c5-ba24-39143c0f90fb"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (69097-829-05)", "package_ndc": "69097-829-05", "marketing_start_date": "20160720"}], "brand_name": "Quinapril and Hydrochlorothiazide 20/12.5", "product_id": "69097-829_4d3f7e7a-ed61-4df6-bc45-f38fb4117406", "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": "69097-829", "generic_name": "Quinapril and Hydrochlorothiazide 20/12.5", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril and Hydrochlorothiazide 20/12.5", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "QUINAPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA201356", "marketing_category": "ANDA", "marketing_start_date": "20160720", "listing_expiration_date": "20261231"}