Package 43063-679-30

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-679-30
Digits Only 4306367930
Product NDC 43063-679
Product ID 43063-679_2fb065bb-3ffc-7a24-e063-6294a90a7352
Description

30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-679-30)

Marketing

Marketing Status
Marketed Since 2016-06-09
Brand benazepril hydrochloride
Generic benazepril hydrochloride
Sample Package No

Linked Drug Pages (1)

Benazepril Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2fb065bb-3ffc-7a24-e063-6294a90a7352", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687"], "spl_set_id": ["355811f0-2885-0d49-e054-00144ff8d46c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-679-30)", "package_ndc": "43063-679-30", "marketing_start_date": "20160609"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-679-90)", "package_ndc": "43063-679-90", "marketing_start_date": "20240607"}], "brand_name": "Benazepril Hydrochloride", "product_id": "43063-679_2fb065bb-3ffc-7a24-e063-6294a90a7352", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "43063-679", "generic_name": "Benazepril Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}