61442-201 NDC - CEPHALEXIN ()

Drug Information

Product NDC: 61442-201

Proprietary Name: Cephalexin

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Carlsbad Technology, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/1/2009

Package Information

No. Package Code Package Description Billing Unit
161442-201-0124 BOTTLE in 1 BOX (61442-201-01) / 100 mL in 1 BOTTLEML
261442-201-0224 BOTTLE in 1 BOX (61442-201-02) / 200 mL in 1 BOTTLEML

NDC Record

Field Name Field Value Definition
PRODUCT NDC61442-201The 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 NAMECephalexinThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/1/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECarlsbad Technology, Inc.Name 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