Package 65862-471-90

Brand: fosinopril sodium

Generic: fosinopril sodium
NDC Package

Package Facts

Identity

Package NDC 65862-471-90
Digits Only 6586247190
Product NDC 65862-471
Description

90 TABLET in 1 BOTTLE (65862-471-90)

Marketing

Marketing Status
Marketed Since 2011-03-30
Brand fosinopril sodium
Generic fosinopril sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f6a2e63b-e4fb-46c3-8687-eec210b347c4", "openfda": {"upc": ["0365862471307", "0365862472304", "0365862473301"], "unii": ["NW2RTH6T2N"], "rxcui": ["857169", "857183", "857187"], "spl_set_id": ["aee04f17-8ee9-42f5-861f-b6ba17220ca4"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (65862-471-30)", "package_ndc": "65862-471-30", "marketing_start_date": "20110330"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65862-471-90)", "package_ndc": "65862-471-90", "marketing_start_date": "20110330"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65862-471-99)", "package_ndc": "65862-471-99", "marketing_start_date": "20110330"}], "brand_name": "Fosinopril Sodium", "product_id": "65862-471_f6a2e63b-e4fb-46c3-8687-eec210b347c4", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "65862-471", "generic_name": "Fosinopril Sodium", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fosinopril Sodium", "active_ingredients": [{"name": "FOSINOPRIL SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA091163", "marketing_category": "ANDA", "marketing_start_date": "20110330", "listing_expiration_date": "20261231"}