NDC 71335-1249 Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
- Product Information
- Product Packages
- Product Characteristics
- What is NDC 71335-1249?
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate Uses
- Active Ingredients UNII Codes
- Inactive Ingredients UNII Codes
- NDC to RxNorm Crosswalk
- Patient Education
Product Information
- 71335 - Bryant Ranch Prepack
- 71335-1249 - Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate
Product Characteristics
Product Packages
NDC Code 71335-1249-1
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 71335-1249-2
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 71335-1249-3
Package Description: 90 TABLET in 1 BOTTLE
NDC Code 71335-1249-4
Package Description: 120 TABLET in 1 BOTTLE
NDC Code 71335-1249-5
Package Description: 18 TABLET in 1 BOTTLE
Product Details
What is NDC 71335-1249?
What are the uses for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate?
Which are Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate UNII Codes?
The UNII codes for the active ingredients in this product are:
- DEXTROAMPHETAMINE SACCHARATE (UNII: G83415V073)
- DEXTROAMPHETAMINE (UNII: TZ47U051FI) (Active Moiety)
- AMPHETAMINE ASPARTATE MONOHYDRATE (UNII: O1ZPV620O4)
- AMPHETAMINE (UNII: CK833KGX7E) (Active Moiety)
- DEXTROAMPHETAMINE SULFATE (UNII: JJ768O327N)
- AMPHETAMINE SULFATE (UNII: 6DPV8NK46S)
Which are Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine 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:
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate?
- RxCUI: 541892 - dextroamphetamine saccharate 2.5 MG / amphetamine aspartate 2.5 MG / dextroamphetamine sulfate 2.5 MG / amphetamine sulfate 2.5 MG Oral Tablet
- RxCUI: 541892 - amphetamine aspartate 2.5 MG / amphetamine sulfate 2.5 MG / dextroamphetamine saccharate 2.5 MG / dextroamphetamine sulfate 2.5 MG Oral Tablet
- RxCUI: 541892 - mixed amphetamine salts 10 MG Oral Tablet
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Patient Education
Dextroamphetamine and Amphetamine
The combination of dextroamphetamine and amphetamine (Adderall, Adderall XR, Mydayis) 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). Adderall is used to treat ADHD in adults and children 3 years of age and older. Adderall XR is used to treat ADHD in adults and children 6 years of age and older. Mydayis is used to treat ADHD in adults and children 13 years of age and older. Dextroamphetamine and amphetamine (Adderall) is also used to treat narcolepsy (a sleep disorder that causes excessive daytime sleepiness and sudden attacks of sleep) in adults and children 12 years of age and older. The combination of dextroamphetamine and amphetamine 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".