FDA NDC Directory · JSON-LD · Markdown

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, Amphetamine Sulfate

NDC 55466-131 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNeolpharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210754
Dosage form / routeTABLET · ORAL
Active ingredientsAMPHETAMINE ASPARTATE (3.75 mg/1)
AMPHETAMINE SULFATE (3.75 mg/1)
DEXTROAMPHETAMINE SACCHARATE (3.75 mg/1)
DEXTROAMPHETAMINE SULFATE (3.75 mg/1)
Marketing started20250205
Package count1

External sources

Source: openFDA. Public-domain (CC0).