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Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate

NDC 57664-951 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215997
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsAMPHETAMINE ASPARTATE MONOHYDRATE (6.25 mg/1)
AMPHETAMINE SULFATE (6.25 mg/1)
DEXTROAMPHETAMINE SACCHARATE (6.25 mg/1)
DEXTROAMPHETAMINE SULFATE (6.25 mg/1)
Marketing started20240201
Package count1

External sources

Source: openFDA. Public-domain (CC0).