53014-531 NDC - METHYLPHENIDATE HYDROCHLORIDE ()

Drug Information

Product NDC: 53014-531

Proprietary Name: Methylphenidate Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Unither Manufacturing, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/4/1979

Package Information

No. Package Code Package Description Billing Unit
153014-531-07100 TABLET in 1 BOTTLE (53014-531-07)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC53014-531The 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 NAMEMethylphenidate HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/4/1979This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEUnither Manufacturing, LLCName 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