Package 68071-1770-1

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-1770-1
Digits Only 6807117701
Product NDC 68071-1770
Product ID 68071-1770_2d82d6ea-a2a6-ec64-e063-6294a90a3d04
Description

100 TABLET, COATED in 1 BOTTLE (68071-1770-1)

Marketing

Marketing Status
Marketed Since 2017-08-02
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": "2d82d6ea-a2a6-ec64-e063-6294a90a3d04", "openfda": {"upc": ["0368071177015"], "unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["55c99902-3d4d-05e9-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (68071-1770-1)", "package_ndc": "68071-1770-1", "marketing_start_date": "20170802"}], "brand_name": "Benazepril Hydrochloride", "product_id": "68071-1770_2d82d6ea-a2a6-ec64-e063-6294a90a3d04", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68071-1770", "generic_name": "Benazepril Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}