Package 51655-737-52

Brand: quinapril

Generic: quinapril
NDC Package

Package Facts

Identity

Package NDC 51655-737-52
Digits Only 5165573752
Product NDC 51655-737
Product ID 51655-737_49514d2d-e05b-44ba-e063-6394a90ad56a
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-737-52)

Marketing

Marketing Status
Marketed Since 2021-07-19
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": "49514d2d-e05b-44ba-e063-6394a90ad56a", "openfda": {"unii": ["33067B3N2M"], "rxcui": ["314203"], "spl_set_id": ["da562e3b-4411-e750-e053-2a95a90ad7e5"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-737-52)", "package_ndc": "51655-737-52", "marketing_start_date": "20210719"}], "brand_name": "Quinapril", "product_id": "51655-737_49514d2d-e05b-44ba-e063-6394a90ad56a", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "51655-737", "generic_name": "Quinapril", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA077690", "marketing_category": "ANDA", "marketing_start_date": "20210719", "listing_expiration_date": "20271231"}