fosinopril sodium

Generic: fosinopril sodium

Labeler: exelan pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fosinopril sodium
Generic Name fosinopril sodium
Labeler exelan pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fosinopril sodium 40 mg/1

Manufacturer
Exelan Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 76282-202
Product ID 76282-202_ed121c1b-359c-471e-913c-4afdf9102c34
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077222
Listing Expiration 2026-12-31
Marketing Start 2005-06-21

Pharmacologic Class

Classes
angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76282202
Hyphenated Format 76282-202

Supplemental Identifiers

RxCUI
857169 857183 857187
UPC
0376282202907 0376282201900 0376282200903
UNII
NW2RTH6T2N

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name fosinopril sodium (source: ndc)
Generic Name fosinopril sodium (source: ndc)
Application Number ANDA077222 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (76282-202-10)
  • 90 TABLET in 1 BOTTLE (76282-202-90)
source: ndc

Packages (2)

76282-202-10 1000 TABLET in 1 BOTTLE (76282-202-10) 76282-202-90 90 TABLET in 1 BOTTLE (76282-202-90)

Ingredients (1)

fosinopril sodium (40 mg/1)

Linked Drug Pages (1)

Fosinopril sodium ndc-match (0.9)

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 (76282-202-10)", "package_ndc": "76282-202-10", "marketing_start_date": "20050621"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76282-202-90)", "package_ndc": "76282-202-90", "marketing_start_date": "20050621"}], "brand_name": "Fosinopril sodium", "product_id": "76282-202_ed121c1b-359c-471e-913c-4afdf9102c34", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "76282-202", "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": "40 mg/1"}], "application_number": "ANDA077222", "marketing_category": "ANDA", "marketing_start_date": "20050621", "listing_expiration_date": "20261231"}