Package 69097-857-15

Brand: fosinopril sodium

Generic: fosinopril
NDC Package

Package Facts

Identity

Package NDC 69097-857-15
Digits Only 6909785715
Product NDC 69097-857
Description

1000 TABLET in 1 BOTTLE (69097-857-15)

Marketing

Marketing Status
Marketed Since 2016-06-16
Brand fosinopril sodium
Generic fosinopril
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6d672087-9b6a-4afe-8c3e-0616943a82cf", "openfda": {"upc": ["0369097857059", "0369097856052", "0369097858056"], "unii": ["NW2RTH6T2N"], "rxcui": ["857169", "857183", "857187"], "spl_set_id": ["736fe52f-69fb-48b2-b1c5-f06531878538"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (69097-857-05)", "package_ndc": "69097-857-05", "marketing_start_date": "20160616"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69097-857-15)", "package_ndc": "69097-857-15", "marketing_start_date": "20160616"}], "brand_name": "Fosinopril Sodium", "product_id": "69097-857_6d672087-9b6a-4afe-8c3e-0616943a82cf", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "69097-857", "generic_name": "Fosinopril", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fosinopril Sodium", "active_ingredients": [{"name": "FOSINOPRIL SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA077222", "marketing_category": "ANDA", "marketing_start_date": "20160616", "listing_expiration_date": "20261231"}