Package 71335-1707-1

Brand: quinapril

Generic: quinapril
NDC Package

Package Facts

Identity

Package NDC 71335-1707-1
Digits Only 7133517071
Product NDC 71335-1707
Product ID 71335-1707_ac824409-47c6-4f5c-b68a-87cb2806af8c
Description

30 TABLET in 1 BOTTLE (71335-1707-1)

Marketing

Marketing Status
Marketed Since 2020-09-10
Brand quinapril
Generic quinapril
Sample Package No

Linked Drug Pages (1)

Quinapril ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ac824409-47c6-4f5c-b68a-87cb2806af8c", "openfda": {"unii": ["33067B3N2M"], "rxcui": ["312748"], "spl_set_id": ["a6cf2ffd-cf94-4f1c-a12e-ce0e93a6304d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1707-1)", "package_ndc": "71335-1707-1", "marketing_start_date": "20200910"}], "brand_name": "Quinapril", "product_id": "71335-1707_ac824409-47c6-4f5c-b68a-87cb2806af8c", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "71335-1707", "generic_name": "Quinapril", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077690", "marketing_category": "ANDA", "marketing_start_date": "20070226", "listing_expiration_date": "20261231"}