Package 68001-188-05

Brand: quinapril

Generic: quinapril
NDC Package

Package Facts

Identity

Package NDC 68001-188-05
Digits Only 6800118805
Product NDC 68001-188
Product ID 68001-188_df08337a-79bd-47c9-858a-8ee32469cfe5
Description

90 TABLET in 1 BOTTLE (68001-188-05)

Marketing

Marketing Status
Marketed Since 2014-02-25
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": "df08337a-79bd-47c9-858a-8ee32469cfe5", "openfda": {"unii": ["33067B3N2M"], "rxcui": ["312748", "312749", "312750", "314203"], "spl_set_id": ["1b5809a8-873d-44cb-af59-e0d8fc81b385"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68001-188-05)", "package_ndc": "68001-188-05", "marketing_start_date": "20140225"}], "brand_name": "Quinapril", "product_id": "68001-188_df08337a-79bd-47c9-858a-8ee32469cfe5", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "68001-188", "generic_name": "Quinapril", "labeler_name": "BluePoint Laboratories", "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": "20140225", "listing_expiration_date": "20261231"}