57721-671 NDC - AMILORIDE HYDROCHLORIDE ()

Drug Information

Product NDC: 57721-671

Proprietary Name: amiloride hydrochloride

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	57721-671-01	100 TABLET in 1 BOTTLE (57721-671-01)
2	57721-671-05	500 TABLET in 1 BOTTLE (57721-671-05)
3	57721-671-06	30 TABLET in 1 BOTTLE (57721-671-06)
4	57721-671-10	1000 TABLET in 1 BOTTLE (57721-671-10)
5	57721-671-16	90 TABLET in 1 BOTTLE (57721-671-16)
6	57721-671-30	10 BLISTER PACK in 1 CARTON (57721-671-30) / 10 TABLET in 1 BLISTER PACK

Field Name	Field Value	Definition
PRODUCT NDC	57721-671	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	amiloride hydrochloride	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	12/1/2021	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	WINDLAS BIOTECH LIMITED	Name of Company corresponding to the labeler code segment of the Product NDC.

Export to text format icon Download this NDC record in Text format: Export

Export to text format icon Download this NDC record in Excel (CSV) format: Export

Export to text format icon Download this NDC record in XML format: Export

This page was last updated on: 4/12/2024