Package 63187-874-60

Brand: quinapril

Generic: quinapril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63187-874-60
Digits Only 6318787460
Product NDC 63187-874
Description

60 TABLET, FILM COATED in 1 BOTTLE (63187-874-60)

Marketing

Marketing Status
Marketed Since 2017-08-01
Brand quinapril
Generic quinapril hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47f95e90-75fb-4294-b861-9a2349a48e91", "openfda": {"unii": ["33067B3N2M"], "rxcui": ["312748"], "spl_set_id": ["42e4f9dd-6032-4257-bd0f-8e9b71027f03"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-874-30)", "package_ndc": "63187-874-30", "marketing_start_date": "20170801"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-874-60)", "package_ndc": "63187-874-60", "marketing_start_date": "20170801"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-874-90)", "package_ndc": "63187-874-90", "marketing_start_date": "20170801"}], "brand_name": "Quinapril", "product_id": "63187-874_47f95e90-75fb-4294-b861-9a2349a48e91", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "63187-874", "generic_name": "Quinapril Hydrochloride", "labeler_name": "Proficient Rx LP", "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"}