Package 0574-0292-01

Brand: amiloride hydrochloride

Generic: amiloride hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0574-0292-01
Digits Only 0574029201
Product NDC 0574-0292
Product ID 0574-0292_416c3aaf-7390-40cf-995a-31258156b4f2
Description

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

Marketing

Marketing Status
Marketed Since 2009-04-06
Brand amiloride hydrochloride
Generic amiloride hydrochloride
Sample Package No

Linked Drug Pages (1)

amiloride hydrochloride ndc-match (0.95)

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"}