quinapril

Generic: quinapril

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quinapril
Generic Name quinapril
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

quinapril hydrochloride 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-8710
Product ID 63629-8710_78872c13-1caa-4a0f-9f5e-995fcfb35e73
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205823
Listing Expiration 2026-12-31
Marketing Start 2017-11-10

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 636298710
Hyphenated Format 63629-8710

Supplemental Identifiers

RxCUI
312749
UNII
33067B3N2M

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 ANDA205823 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (63629-8710-1)
source: ndc

Packages (1)

63629-8710-1 30 TABLET in 1 BOTTLE (63629-8710-1)

Ingredients (1)

quinapril hydrochloride (20 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": "78872c13-1caa-4a0f-9f5e-995fcfb35e73", "openfda": {"unii": ["33067B3N2M"], "rxcui": ["312749"], "spl_set_id": ["da84cb14-a9dd-4df0-a7e5-d5fbd84ac6da"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-8710-1)", "package_ndc": "63629-8710-1", "marketing_start_date": "20210802"}], "brand_name": "QUINAPRIL", "product_id": "63629-8710_78872c13-1caa-4a0f-9f5e-995fcfb35e73", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "63629-8710", "generic_name": "quinapril", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "QUINAPRIL", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA205823", "marketing_category": "ANDA", "marketing_start_date": "20171110", "listing_expiration_date": "20261231"}