Package 60760-352-90

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-352-90
Digits Only 6076035290
Product NDC 60760-352
Product ID 60760-352_7a024766-f7af-7685-e053-2a91aa0ab774
Description

90 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-352-90)

Marketing

Marketing Status
Marketed Since 2017-11-15
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": "7a024766-f7af-7685-e053-2a91aa0ab774", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898690"], "spl_set_id": ["5e9a61dd-9b2e-5b86-e053-2a91aa0a365c"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-352-90)", "package_ndc": "60760-352-90", "marketing_start_date": "20171115"}], "brand_name": "Benazepril Hydrochloride", "product_id": "60760-352_7a024766-f7af-7685-e053-2a91aa0ab774", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "60760-352", "generic_name": "Benazepril Hydrochloride", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}