68382-953 NDC - DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE ()

Drug Information

Product NDC: 68382-953

Proprietary Name: Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/31/2017

Package Information

No. Package Code Package Description Billing Unit
168382-953-01100 TABLET in 1 BOTTLE (68382-953-01)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC68382-953The 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 NAMEDextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine SulfateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/31/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEZydus Pharmaceuticals (USA) Inc.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