17856-0032 NDC - LETROZOLE ()

Drug Information

Product NDC: 17856-0032

Proprietary Name: Letrozole

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ATLANTIC BIOLOGICALS CORP.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/13/2020

Package Information

No. Package Code Package Description Billing Unit
117856-0032-1100 POUCH in 1 BOX, UNIT-DOSE (17856-0032-1) / 1 TABLET, FILM COATED in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC17856-0032The 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 NAMELetrozoleThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/13/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEATLANTIC BIOLOGICALS CORP.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