quinapril

Generic: quinapril hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quinapril
Generic Name quinapril hydrochloride
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

quinapril hydrochloride 10 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-618
Product ID 65862-618_5263abd5-ce46-4918-9bb0-9632861bcbc9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202725
Listing Expiration 2026-12-31
Marketing Start 2013-04-29

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 65862618
Hyphenated Format 65862-618

Supplemental Identifiers

RxCUI
312748 312749 312750 314203
UPC
0365862618900 0365862617903 0365862619907
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 hydrochloride (source: ndc)
Application Number ANDA202725 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (65862-618-30)
  • 15000 TABLET, FILM COATED in 1 BOTTLE (65862-618-55)
  • 10 BLISTER PACK in 1 CARTON (65862-618-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-618-10)
  • 90 TABLET, FILM COATED in 1 BOTTLE (65862-618-90)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (65862-618-99)
source: ndc

Packages (5)

65862-618-30 30 TABLET, FILM COATED in 1 BOTTLE (65862-618-30) 65862-618-55 15000 TABLET, FILM COATED in 1 BOTTLE (65862-618-55) 65862-618-78 10 BLISTER PACK in 1 CARTON (65862-618-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-618-10) 65862-618-90 90 TABLET, FILM COATED in 1 BOTTLE (65862-618-90) 65862-618-99 1000 TABLET, FILM COATED in 1 BOTTLE (65862-618-99)

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": "5263abd5-ce46-4918-9bb0-9632861bcbc9", "openfda": {"upc": ["0365862618900", "0365862617903", "0365862619907"], "unii": ["33067B3N2M"], "rxcui": ["312748", "312749", "312750", "314203"], "spl_set_id": ["93e6e668-5306-4f26-81d8-cbc3a7a5e787"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-618-30)", "package_ndc": "65862-618-30", "marketing_start_date": "20130429"}, {"sample": false, "description": "15000 TABLET, FILM COATED in 1 BOTTLE (65862-618-55)", "package_ndc": "65862-618-55", "marketing_start_date": "20130429"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-618-78)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-618-10)", "package_ndc": "65862-618-78", "marketing_start_date": "20130429"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-618-90)", "package_ndc": "65862-618-90", "marketing_start_date": "20130429"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-618-99)", "package_ndc": "65862-618-99", "marketing_start_date": "20130429"}], "brand_name": "Quinapril", "product_id": "65862-618_5263abd5-ce46-4918-9bb0-9632861bcbc9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "65862-618", "generic_name": "Quinapril Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202725", "marketing_category": "ANDA", "marketing_start_date": "20130429", "listing_expiration_date": "20261231"}