fosinopril sodium

Generic: fosinopril sodium

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fosinopril sodium
Generic Name fosinopril sodium
Labeler aurobindo pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fosinopril sodium 40 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-473
Product ID 65862-473_f6a2e63b-e4fb-46c3-8687-eec210b347c4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091163
Listing Expiration 2026-12-31
Marketing Start 2011-03-30

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 65862473
Hyphenated Format 65862-473

Supplemental Identifiers

RxCUI
857169 857183 857187
UPC
0365862471307 0365862472304 0365862473301
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 ANDA091163 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (65862-473-30)
  • 90 TABLET in 1 BOTTLE (65862-473-90)
  • 1000 TABLET in 1 BOTTLE (65862-473-99)
source: ndc

Packages (3)

65862-473-30 30 TABLET in 1 BOTTLE (65862-473-30) 65862-473-90 90 TABLET in 1 BOTTLE (65862-473-90) 65862-473-99 1000 TABLET in 1 BOTTLE (65862-473-99)

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": "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 (65862-473-30)", "package_ndc": "65862-473-30", "marketing_start_date": "20110330"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65862-473-90)", "package_ndc": "65862-473-90", "marketing_start_date": "20110330"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65862-473-99)", "package_ndc": "65862-473-99", "marketing_start_date": "20110330"}], "brand_name": "Fosinopril Sodium", "product_id": "65862-473_f6a2e63b-e4fb-46c3-8687-eec210b347c4", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "65862-473", "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": "40 mg/1"}], "application_number": "ANDA091163", "marketing_category": "ANDA", "marketing_start_date": "20110330", "listing_expiration_date": "20261231"}