fosinopril sodium
Generic: fosinopirl sodium
Labeler: solco healthcare llcDrug Facts
Product Profile
Brand Name
fosinopril sodium
Generic Name
fosinopirl sodium
Labeler
solco healthcare llc
Dosage Form
TABLET
Routes
Active Ingredients
fosinopril sodium 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43547-386
Product ID
43547-386_e39b61db-42b8-4ddf-89d1-549c08d49e71
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205670
Listing Expiration
2026-12-31
Marketing Start
2017-10-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43547386
Hyphenated Format
43547-386
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
fosinopirl sodium (source: ndc)
Application Number
ANDA205670 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (43547-386-09)
- 1000 TABLET in 1 BOTTLE (43547-386-11)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e39b61db-42b8-4ddf-89d1-549c08d49e71", "openfda": {"upc": ["0343547387099"], "unii": ["NW2RTH6T2N"], "rxcui": ["857169", "857183", "857187"], "spl_set_id": ["0a66f606-5e6f-473d-8a1e-9ef316adb2e2"], "manufacturer_name": ["Solco Healthcare LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (43547-386-09)", "package_ndc": "43547-386-09", "marketing_start_date": "20171001"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (43547-386-11)", "package_ndc": "43547-386-11", "marketing_start_date": "20171001"}], "brand_name": "Fosinopril sodium", "product_id": "43547-386_e39b61db-42b8-4ddf-89d1-549c08d49e71", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "43547-386", "generic_name": "fosinopirl sodium", "labeler_name": "Solco Healthcare LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fosinopril sodium", "active_ingredients": [{"name": "FOSINOPRIL SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA205670", "marketing_category": "ANDA", "marketing_start_date": "20171001", "listing_expiration_date": "20261231"}