quinapril

Generic: quinapril

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quinapril
Generic Name quinapril
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

quinapril hydrochloride 40 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-737
Product ID 51655-737_49514d2d-e05b-44ba-e063-6394a90ad56a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077690
Listing Expiration 2027-12-31
Marketing Start 2021-07-19

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 51655737
Hyphenated Format 51655-737

Supplemental Identifiers

RxCUI
314203
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 ANDA077690 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (51655-737-52)
source: ndc

Packages (1)

51655-737-52 30 TABLET in 1 BOTTLE, PLASTIC (51655-737-52)

Ingredients (1)

quinapril hydrochloride (40 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": "49514d2d-e05b-44ba-e063-6394a90ad56a", "openfda": {"unii": ["33067B3N2M"], "rxcui": ["314203"], "spl_set_id": ["da562e3b-4411-e750-e053-2a95a90ad7e5"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-737-52)", "package_ndc": "51655-737-52", "marketing_start_date": "20210719"}], "brand_name": "Quinapril", "product_id": "51655-737_49514d2d-e05b-44ba-e063-6394a90ad56a", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "51655-737", "generic_name": "Quinapril", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA077690", "marketing_category": "ANDA", "marketing_start_date": "20210719", "listing_expiration_date": "20271231"}