Package 49884-117-10

Brand: amiloride hydrochloride

Generic: amiloride hydrochloride
NDC Package

Package Facts

Identity

Package NDC 49884-117-10
Digits Only 4988411710
Product NDC 49884-117
Product ID 49884-117_cee18f3c-6f68-46d0-9e69-72c504c5a798
Description

1000 TABLET in 1 BOTTLE (49884-117-10)

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": "cee18f3c-6f68-46d0-9e69-72c504c5a798", "openfda": {"upc": ["0349884117108"], "unii": ["7M458Q65S3"], "rxcui": ["977880"], "spl_set_id": ["e0cc2d44-436a-47e8-a890-589882fff4c4"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (49884-117-01)", "package_ndc": "49884-117-01", "marketing_start_date": "19860512"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (49884-117-10)", "package_ndc": "49884-117-10", "marketing_start_date": "19860512"}], "brand_name": "Amiloride Hydrochloride", "product_id": "49884-117_cee18f3c-6f68-46d0-9e69-72c504c5a798", "dosage_form": "TABLET", "pharm_class": ["Decreased Renal K+ Excretion [PE]", "Increased Diuresis [PE]", "Potassium-sparing Diuretic [EPC]"], "product_ndc": "49884-117", "generic_name": "Amiloride Hydrochloride", "labeler_name": "Endo USA, Inc.", "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"}