Package 68788-6889-1

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-6889-1
Digits Only 6878868891
Product NDC 68788-6889
Description

100 TABLET, COATED in 1 BOTTLE (68788-6889-1)

Marketing

Marketing Status
Marketed Since 2017-02-06
Brand benazepril hydrochloride
Generic benazepril hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30fc5f8d-61ca-4b67-9cb8-fbba48a8a2b0", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898723"], "spl_set_id": ["01a3c9f6-41aa-47a7-8c56-5462c6b54416"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (68788-6889-1)", "package_ndc": "68788-6889-1", "marketing_start_date": "20170206"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (68788-6889-3)", "package_ndc": "68788-6889-3", "marketing_start_date": "20170206"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68788-6889-6)", "package_ndc": "68788-6889-6", "marketing_start_date": "20170206"}, {"sample": false, "description": "120 TABLET, COATED in 1 BOTTLE (68788-6889-8)", "package_ndc": "68788-6889-8", "marketing_start_date": "20170206"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (68788-6889-9)", "package_ndc": "68788-6889-9", "marketing_start_date": "20170206"}], "brand_name": "Benazepril Hydrochloride", "product_id": "68788-6889_30fc5f8d-61ca-4b67-9cb8-fbba48a8a2b0", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68788-6889", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20170206", "listing_expiration_date": "20271231"}