Package 76282-201-90
Brand: fosinopril sodium
Generic: fosinopril sodiumPackage Facts
Identity
Package NDC
76282-201-90
Digits Only
7628220190
Product NDC
76282-201
Description
90 TABLET in 1 BOTTLE (76282-201-90)
Marketing
Marketing Status
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": "ed121c1b-359c-471e-913c-4afdf9102c34", "openfda": {"upc": ["0376282202907", "0376282201900", "0376282200903"], "unii": ["NW2RTH6T2N"], "rxcui": ["857169", "857183", "857187"], "spl_set_id": ["e2ff3171-a17a-456a-9272-ca1682b01d19"], "manufacturer_name": ["Exelan Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (76282-201-10)", "package_ndc": "76282-201-10", "marketing_start_date": "20050621"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76282-201-90)", "package_ndc": "76282-201-90", "marketing_start_date": "20050621"}], "brand_name": "Fosinopril sodium", "product_id": "76282-201_ed121c1b-359c-471e-913c-4afdf9102c34", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "76282-201", "generic_name": "Fosinopril sodium", "labeler_name": "Exelan Pharmaceuticals, 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": "20050621", "listing_expiration_date": "20261231"}