60723-010 NDC - MONTELUKAST SODIUM ()

Drug Information

Product NDC: 60723-010

Proprietary Name: Montelukast Sodium

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Hangzhou Minsheng Binjiang Pharm
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/30/2016

Package Information

No. Package Code Package Description Billing Unit
160723-010-0330 TABLET in 1 BOTTLE (60723-010-03)
260723-010-0990 TABLET in 1 BOTTLE (60723-010-09)
360723-010-50500 TABLET in 1 BOTTLE (60723-010-50)

NDC Record

Field Name Field Value Definition
PRODUCT NDC60723-010The 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 NAMEMontelukast SodiumThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/30/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEHangzhou Minsheng Binjiang PharmName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023