50090-3967 NDC - OLANZAPINE ()

Drug Information

Product NDC: 50090-3967

Proprietary Name: Olanzapine

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: A-S Medication Solutions
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/24/2011

Package Information

No. Package Code Package Description Billing Unit
150090-3967-03 BLISTER PACK in 1 CARTON (50090-3967-0) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Record

Field Name Field Value Definition
PRODUCT NDC50090-3967The 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 NAMEOlanzapineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/24/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEA-S Medication SolutionsName 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