quinapril

Generic: quinapril

Labeler: solco healthcare us, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quinapril
Generic Name quinapril
Labeler solco healthcare us, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

quinapril hydrochloride 20 mg/1

Manufacturer
Solco Healthcare US, LLC

Identifiers & Regulatory

Product NDC 43547-412
Product ID 43547-412_b8f1731a-cbac-4f64-a8d4-320b80b335e1
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 43547412
Hyphenated Format 43547-412

Supplemental Identifiers

RxCUI
312748 312749 312750 314203
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 ANDA205823 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (43547-412-09)
source: ndc

Packages (1)

43547-412-09 90 TABLET in 1 BOTTLE (43547-412-09)

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": "b8f1731a-cbac-4f64-a8d4-320b80b335e1", "openfda": {"unii": ["33067B3N2M"], "rxcui": ["312748", "312749", "312750", "314203"], "spl_set_id": ["cd46691d-5593-4a9f-a937-999c6803e312"], "manufacturer_name": ["Solco Healthcare US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (43547-412-09)", "package_ndc": "43547-412-09", "marketing_start_date": "20171110"}], "brand_name": "QUINAPRIL", "product_id": "43547-412_b8f1731a-cbac-4f64-a8d4-320b80b335e1", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "43547-412", "generic_name": "quinapril", "labeler_name": "Solco Healthcare US, LLC", "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"}