fosinopril sodium

Generic: fosinopril

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fosinopril sodium
Generic Name fosinopril
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fosinopril sodium 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0381
Product ID 71335-0381_45aabe20-10c6-4b99-989a-2b64bd266114
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 713350381
Hyphenated Format 71335-0381

Supplemental Identifiers

RxCUI
857169
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 (71335-0381-1)
  • 90 TABLET in 1 BOTTLE (71335-0381-2)
  • 60 TABLET in 1 BOTTLE (71335-0381-3)
  • 28 TABLET in 1 BOTTLE (71335-0381-4)
source: ndc

Packages (4)

Ingredients (1)

fosinopril sodium (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45aabe20-10c6-4b99-989a-2b64bd266114", "openfda": {"unii": ["NW2RTH6T2N"], "rxcui": ["857169"], "spl_set_id": ["fc38f1bb-f175-4a81-8ed9-c8701efdea35"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0381-1)", "package_ndc": "71335-0381-1", "marketing_start_date": "20220209"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0381-2)", "package_ndc": "71335-0381-2", "marketing_start_date": "20220209"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0381-3)", "package_ndc": "71335-0381-3", "marketing_start_date": "20220209"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-0381-4)", "package_ndc": "71335-0381-4", "marketing_start_date": "20220209"}], "brand_name": "Fosinopril Sodium", "product_id": "71335-0381_45aabe20-10c6-4b99-989a-2b64bd266114", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "71335-0381", "generic_name": "Fosinopril", "labeler_name": "Bryant Ranch Prepack", "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"}