NDC 68382-942 Dextroamphetamine Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68382 - Zydus Pharmaceuticals (usa) Inc.
- 68382-942 - Dextroamphetamine Sulfate
Product Characteristics
PINK (C48328)
N942
Product Packages
Product Details
What is NDC 68382-942?
What are the uses for Dextroamphetamine Sulfate?
Which are Dextroamphetamine Sulfate UNII Codes?
The UNII codes for the active ingredients in this product are:
- DEXTROAMPHETAMINE SULFATE (UNII: JJ768O327N)
- DEXTROAMPHETAMINE (UNII: TZ47U051FI) (Active Moiety)
Which are Dextroamphetamine Sulfate Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- CALCIUM SULFATE (UNII: WAT0DDB505)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SUCROSE (UNII: C151H8M554)
- STARCH, CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Dextroamphetamine Sulfate?
- RxCUI: 884385 - dextroamphetamine sulfate 10 MG Oral Tablet
- RxCUI: 884386 - dextroamphetamine sulfate 5 MG Oral Tablet
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Patient Education
Dextroamphetamine
Dextroamphetamine is used as part of a treatment program to control symptoms of attention deficit hyperactivity disorder (ADHD; more difficulty focusing, controlling actions, and remaining still or quiet than other people who are the same age) in adults and children. Dextroamphetamine is also used to treat narcolepsy (a sleep disorder that causes excessive daytime sleepiness and sudden attacks of sleep). Dextroamphetamine is in a class of medications called central nervous system stimulants. It works by changing the amounts of certain natural substances in the brain.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".