← FDA DRUG APPROVALS

FDA ANDA · ANDA213583

AMPHETAMINE SULFATE

Sponsor: SPECGX LLC

APPLICATION
ANDA213583
TYPE
ANDA
ORIGINAL APPROVAL
2021-01-22
LATEST ACTION
2023-10-18
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Prescription

Products

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

Approval history

2023-10-18Labeling · Supplement 3 · standardAP
2022-02-25Labeling · Supplement 2 · standardAP
2021-01-22UNKNOWN · Original · standardAP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

Pharma industryGMP disciplineFDA drug shortagesFDA enforcement & recalls

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.

Weekly Briefing

Get the Weekly GxP Briefing

Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.

Read a past issue →