64679-572 NDC - RISPERIDONE ()

Drug Information

Product NDC: 64679-572

Proprietary Name: Risperidone

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Wockhardt USA LLC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/9/2008

Package Information

No. Package Code Package Description Billing Unit
164679-572-0130 TABLET, FILM COATED in 1 BOTTLE (64679-572-01)
264679-572-02500 TABLET, FILM COATED in 1 BOTTLE (64679-572-02)EA
364679-572-03100 BLISTER PACK in 1 CARTON (64679-572-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK
464679-572-0460 TABLET, FILM COATED in 1 BOTTLE (64679-572-04)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC64679-572The 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 NAMERisperidoneThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/9/2008This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWockhardt USA LLC.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