Package 63629-2114-1

Brand: amiloride hydrochloride

Generic: amiloride hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2114-1
Digits Only 6362921141
Product NDC 63629-2114
Product ID 63629-2114_84adc61b-3ed3-452d-a1b8-d062869b263d
Description

1000 TABLET in 1 BOTTLE (63629-2114-1)

Marketing

Marketing Status
Marketed Since 1986-05-12
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": "84adc61b-3ed3-452d-a1b8-d062869b263d", "openfda": {"unii": ["7M458Q65S3"], "rxcui": ["977880"], "spl_set_id": ["18d551a9-ffc7-4b14-adbd-92d84aa8e966"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (63629-2114-1)", "package_ndc": "63629-2114-1", "marketing_start_date": "19860512"}], "brand_name": "Amiloride Hydrochloride", "product_id": "63629-2114_84adc61b-3ed3-452d-a1b8-d062869b263d", "dosage_form": "TABLET", "pharm_class": ["Decreased Renal K+ Excretion [PE]", "Increased Diuresis [PE]", "Potassium-sparing Diuretic [EPC]"], "product_ndc": "63629-2114", "generic_name": "Amiloride Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amiloride Hydrochloride", "active_ingredients": [{"name": "AMILORIDE HYDROCHLORIDE ANHYDROUS", "strength": "5 mg/1"}], "application_number": "ANDA070346", "marketing_category": "ANDA", "marketing_start_date": "19860122", "listing_expiration_date": "20261231"}