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FDA ANDA · ANDA213852

AMPHETAMINE SULFATE

Sponsor: RHODES PHARMS

APPLICATION
ANDA213852
TYPE
ANDA
ORIGINAL APPROVAL
2021-09-07
LATEST ACTION
2023-10-18
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

AMPHETAMINE SULFATEDiscontinued
AMPHETAMINE SULFATE 5MG · TABLET · ORAL
AMPHETAMINE SULFATEDiscontinued
AMPHETAMINE SULFATE 10MG · TABLET · ORAL

Approval history

2023-10-18Labeling · Supplement 2 · standardAP
2022-02-25Labeling · Supplement 1 · standardAP
2021-09-07UNKNOWN · Original · standardAP
VIEW ON DRUGS@FDA ↗

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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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