fosinopril sodium

Generic: fosinopril

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fosinopril sodium
Generic Name fosinopril
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fosinopril sodium 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2977
Product ID 50090-2977_8f99a421-7303-41b5-bde9-f9beb408fcf8
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 500902977
Hyphenated Format 50090-2977

Supplemental Identifiers

RxCUI
857169 857187
UNII
NW2RTH6T2N

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
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-2977-0)
source: ndc

Packages (1)

50090-2977-0 30 TABLET in 1 BOTTLE (50090-2977-0)

Ingredients (1)

fosinopril sodium (10 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": "8f99a421-7303-41b5-bde9-f9beb408fcf8", "openfda": {"unii": ["NW2RTH6T2N"], "rxcui": ["857169", "857187"], "spl_set_id": ["880e5bf4-ced8-4765-a5c2-2361fd06ed9c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-2977-0)", "package_ndc": "50090-2977-0", "marketing_start_date": "20170418"}], "brand_name": "Fosinopril Sodium", "product_id": "50090-2977_8f99a421-7303-41b5-bde9-f9beb408fcf8", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "50090-2977", "generic_name": "Fosinopril", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fosinopril Sodium", "active_ingredients": [{"name": "FOSINOPRIL SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA077222", "marketing_category": "ANDA", "marketing_start_date": "20160616", "listing_expiration_date": "20261231"}