fosinopril sodium

Generic: fosinopril

Labeler: cipla usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fosinopril sodium
Generic Name fosinopril
Labeler cipla usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fosinopril sodium 20 mg/1

Manufacturer
Cipla USA Inc.

Identifiers & Regulatory

Product NDC 69097-857
Product ID 69097-857_6d672087-9b6a-4afe-8c3e-0616943a82cf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077222
Listing Expiration 2026-12-31
Marketing Start 2016-06-16

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 69097857
Hyphenated Format 69097-857

Supplemental Identifiers

RxCUI
857169 857183 857187
UPC
0369097857059 0369097856052 0369097858056
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 (source: ndc)
Application Number ANDA077222 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (69097-857-05)
  • 1000 TABLET in 1 BOTTLE (69097-857-15)
source: ndc

Packages (2)

69097-857-05 90 TABLET in 1 BOTTLE (69097-857-05) 69097-857-15 1000 TABLET in 1 BOTTLE (69097-857-15)

Ingredients (1)

fosinopril sodium (20 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": "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"}