quinapril

Generic: quinapril

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

Drug Facts

Product Profile

Brand Name quinapril
Generic Name quinapril
Labeler cipla usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

quinapril hydrochloride 10 mg/1

Manufacturer
Cipla USA Inc.

Identifiers & Regulatory

Product NDC 69097-841
Product ID 69097-841_56ce107f-65d9-4ec8-8859-6a256b27dc57
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078457
Listing Expiration 2026-12-31
Marketing Start 2016-07-22

Pharmacologic Class

Classes
angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69097841
Hyphenated Format 69097-841

Supplemental Identifiers

RxCUI
312748 312749 312750 314203
UPC
0369097841058 0369097839055 0369097842055 0369097843052
UNII
33067B3N2M

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 (source: ndc)
Generic Name quinapril (source: ndc)
Application Number ANDA078457 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (69097-841-05)
  • 1000 TABLET in 1 BOTTLE (69097-841-15)
source: ndc

Packages (2)

69097-841-05 90 TABLET in 1 BOTTLE (69097-841-05) 69097-841-15 1000 TABLET in 1 BOTTLE (69097-841-15)

Ingredients (1)

quinapril hydrochloride (10 mg/1)

Linked Drug Pages (1)

Quinapril ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "56ce107f-65d9-4ec8-8859-6a256b27dc57", "openfda": {"upc": ["0369097841058", "0369097839055", "0369097842055", "0369097843052"], "unii": ["33067B3N2M"], "rxcui": ["312748", "312749", "312750", "314203"], "spl_set_id": ["e6d36e1e-8e35-4d06-83dc-45e0456365fd"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (69097-841-05)", "package_ndc": "69097-841-05", "marketing_start_date": "20160722"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69097-841-15)", "package_ndc": "69097-841-15", "marketing_start_date": "20160722"}], "brand_name": "Quinapril", "product_id": "69097-841_56ce107f-65d9-4ec8-8859-6a256b27dc57", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "69097-841", "generic_name": "Quinapril", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078457", "marketing_category": "ANDA", "marketing_start_date": "20160722", "listing_expiration_date": "20261231"}