Package 42794-005-02

Brand: amiloride hydrochloride

Generic: amiloride hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42794-005-02
Digits Only 4279400502
Product NDC 42794-005
Product ID 42794-005_f1f15fe7-63a8-4708-e053-2a95a90a7dea
Description

100 TABLET in 1 BOTTLE (42794-005-02)

Marketing

Marketing Status
Marketed Since 2021-06-14
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": "f1f15fe7-63a8-4708-e053-2a95a90a7dea", "openfda": {"unii": ["7M458Q65S3"], "rxcui": ["977880"], "spl_set_id": ["de12b6f3-3791-4d78-90e6-c487cf951738"], "manufacturer_name": ["Sigmapharm Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42794-005-02)", "package_ndc": "42794-005-02", "marketing_start_date": "20210614"}], "brand_name": "Amiloride Hydrochloride", "product_id": "42794-005_f1f15fe7-63a8-4708-e053-2a95a90a7dea", "dosage_form": "TABLET", "pharm_class": ["Decreased Renal K+ Excretion [PE]", "Increased Diuresis [PE]", "Potassium-sparing Diuretic [EPC]"], "product_ndc": "42794-005", "generic_name": "Amiloride Hydrochloride", "labeler_name": "Sigmapharm Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amiloride Hydrochloride", "active_ingredients": [{"name": "AMILORIDE HYDROCHLORIDE ANHYDROUS", "strength": "5 mg/1"}], "application_number": "ANDA079133", "marketing_category": "ANDA", "marketing_start_date": "20210614", "listing_expiration_date": "20261231"}