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Dextroamphetamine

DEXTROAMPHETAMINE SULFATE

Active ingredient 25 prescription 122 with labelling

Overview

Source: NDC Directory
Ingredient name
DEXTROAMPHETAMINE SULFATE
Base moiety
DEXTROAMPHETAMINE
RxNorm CUI
UNII
JJ768O327N
Medication products
34
Brand names
21
Dosage forms
6
FAERS reports
45,505 · not a risk measure

Products containing this ingredient

Source: NDC Directory 34 products

Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.

By dosage form

How this ingredient is presented across the catalogue.
Dosage form Products Examples
CAPSULE, Extended Release 12 DEXTROAMPHETAMINE SULFATE, DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, and AMPHETAMINE SULFATE, Adderall, DEXEDRINE, Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate …
Tablet 10 Adderall, Dextroamphetamine Saccharate and Amphetamine Aspartate and Dextroamphetamine Sulfate and Amphetamine Sulfate, Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate …
Powder 5 (S)-Alpha-Methylphenethylamine Sulphate, Dextroamphetamine Sulfate, Dextroamphetamine Sulfate Fine NP, Dextroamphetamine Sulfate NP …
Capsule 3 DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE, AMPHETAMINE SULFATE, Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate
Solution 3 dextroamphetamine sulfate, PROCENTRA, Dextroamphetamine
TABLET, Orally Disintegrating 1 Amphetamine Sulfate

Sources for this page

Dataset Agency Used for
NDC Directory FDA Ingredient name, strengths, products, labelers, packages
DailyMed RxNorm mappings NLM RxNorm concept identifier (RxCUI)
FAERS FDA Adverse event report totals