amiloride hydrochloride

Generic: amiloride hydrochloride

Labeler: padagis us llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name amiloride hydrochloride
Generic Name amiloride hydrochloride
Labeler padagis us llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amiloride hydrochloride 5 mg/1

Manufacturer
Padagis US LLC

Identifiers & Regulatory

Product NDC 0574-0292
Product ID 0574-0292_416c3aaf-7390-40cf-995a-31258156b4f2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA018200
Listing Expiration 2026-12-31
Marketing Start 2009-04-06

Pharmacologic Class

Classes
decreased renal k+ excretion [pe] increased diuresis [pe] potassium-sparing diuretic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05740292
Hyphenated Format 0574-0292

Supplemental Identifiers

RxCUI
977880
UNII
FZJ37245UC

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 amiloride hydrochloride (source: ndc)
Generic Name amiloride hydrochloride (source: ndc)
Application Number NDA018200 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0574-0292-01)
source: ndc

Packages (1)

0574-0292-01 100 TABLET in 1 BOTTLE (0574-0292-01)

Ingredients (1)

amiloride hydrochloride (5 mg/1)

Linked Drug Pages (1)

amiloride hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "416c3aaf-7390-40cf-995a-31258156b4f2", "openfda": {"unii": ["FZJ37245UC"], "rxcui": ["977880"], "spl_set_id": ["2b70cf0c-45be-428f-b396-5001ed4e30fc"], "manufacturer_name": ["Padagis US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0574-0292-01)", "package_ndc": "0574-0292-01", "marketing_start_date": "20090406"}], "brand_name": "amiloride hydrochloride", "product_id": "0574-0292_416c3aaf-7390-40cf-995a-31258156b4f2", "dosage_form": "TABLET", "pharm_class": ["Decreased Renal K+ Excretion [PE]", "Increased Diuresis [PE]", "Potassium-sparing Diuretic [EPC]"], "product_ndc": "0574-0292", "generic_name": "amiloride hydrochloride", "labeler_name": "Padagis US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "amiloride hydrochloride", "active_ingredients": [{"name": "AMILORIDE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "NDA018200", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20090406", "listing_expiration_date": "20261231"}