64725-8166 NDC - QUETIAPINE FUMARATE ()

Drug Information

Product NDC: 64725-8166

Proprietary Name: Quetiapine Fumarate

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: TYA Pharmaceuticals
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/27/2012

Package Information

No. Package Code Package Description Billing Unit
164725-8166-1100 TABLET, FILM COATED in 1 BOTTLE (64725-8166-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64725-8166The 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 NAMEQuetiapine FumarateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/27/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMETYA PharmaceuticalsName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 5/20/2020