fosinopril sodium

Generic: fosinopril sodium

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fosinopril sodium
Generic Name fosinopril sodium
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fosinopril sodium 40 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-043
Product ID 62135-043_40d2b698-02dc-4589-e063-6394a90afb52
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076483
Listing Expiration 2026-12-31
Marketing Start 2004-04-23

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 62135043
Hyphenated Format 62135-043

Supplemental Identifiers

RxCUI
857169 857183 857187
UPC
0362135042905 0362135043902 0362135041908
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 ANDA076483 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (62135-043-90)
source: ndc

Packages (1)

62135-043-90 90 TABLET in 1 BOTTLE (62135-043-90)

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": "40d2b698-02dc-4589-e063-6394a90afb52", "openfda": {"upc": ["0362135042905", "0362135043902", "0362135041908"], "unii": ["NW2RTH6T2N"], "rxcui": ["857169", "857183", "857187"], "spl_set_id": ["ff1323cc-7ad8-488d-94a7-a11555db78a7"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-043-90)", "package_ndc": "62135-043-90", "marketing_start_date": "20230601"}], "brand_name": "Fosinopril Sodium", "product_id": "62135-043_40d2b698-02dc-4589-e063-6394a90afb52", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "62135-043", "generic_name": "Fosinopril Sodium", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fosinopril Sodium", "active_ingredients": [{"name": "FOSINOPRIL SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA076483", "marketing_category": "ANDA", "marketing_start_date": "20040423", "listing_expiration_date": "20261231"}