NDC 64380-232 Dextroamphetamine Sulfate

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory .
NDC Product Code:
64380-232
Proprietary Name:
Dextroamphetamine Sulfate
Product Type: [3]
Labeler Code:
64380
Start Marketing Date: [9]
03-24-2024
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
U
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)
BROWN (C48332 - CLEAR)
Shape:
CAPSULE (C48336)
Size(s):
14 MM
16 MM
Imprint(s):
5MG;V2674
10MG;V2675
15MG;V2676
Score:
1

Code Structure Chart

Product Details

What is NDC 64380-232?

The NDC code 64380-232 is assigned by the FDA to the product Dextroamphetamine Sulfate which is product labeled by Strides Pharma Science Limited. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64380-232-01 100 capsule, extended release in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Dextroamphetamine Sulfate?

This medication is used to treat attention deficit hyperactivity disorder - ADHD. It works by changing the amounts of certain natural substances in the brain. Dextroamphetamine belongs to a class of drugs known as stimulants. It can help increase your ability to pay attention, stay focused on an activity, and control behavior problems. It may also help you to organize your tasks and improve listening skills. This medication is also used to treat a certain sleeping disorder (narcolepsy) to help you stay awake during the day. It should not be used to treat tiredness or to hold off sleep in people who do not have a sleep disorder.

Which are Dextroamphetamine Sulfate UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

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Product Footnotes

[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".