quinapril

Generic: quinapril

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quinapril
Generic Name quinapril
Labeler chartwell rx, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

quinapril hydrochloride 40 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-487
Product ID 62135-487_09cd5cb9-4fdf-f133-e063-6294a90af691
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076803
Listing Expiration 2026-12-31
Marketing Start 2005-03-02

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 62135487
Hyphenated Format 62135-487

Supplemental Identifiers

RxCUI
312748 312749 312750 314203
UPC
0362135484606 0362135487904 0362135485900 0362135486907
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 ANDA076803 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (62135-487-90)
source: ndc

Packages (1)

62135-487-90 90 TABLET, FILM COATED in 1 BOTTLE (62135-487-90)

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": "09cd5cb9-4fdf-f133-e063-6294a90af691", "openfda": {"upc": ["0362135484606", "0362135487904", "0362135485900", "0362135486907"], "unii": ["33067B3N2M"], "rxcui": ["312748", "312749", "312750", "314203"], "spl_set_id": ["dbc43dbd-94aa-40e2-a9ea-766110cc8687"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62135-487-90)", "package_ndc": "62135-487-90", "marketing_start_date": "20231106"}], "brand_name": "Quinapril", "product_id": "62135-487_09cd5cb9-4fdf-f133-e063-6294a90af691", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "62135-487", "generic_name": "Quinapril", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA076803", "marketing_category": "ANDA", "marketing_start_date": "20050302", "listing_expiration_date": "20261231"}