← FDA DRUG APPROVALS

FDA ANDA · ANDA218059

ZINC SULFATE

zinc sulfate injection

Sponsor: APOTEX

APPLICATION
ANDA218059
TYPE
ANDA
ORIGINAL APPROVAL
2024-06-10
LATEST ACTION
2024-10-28
ROUTE
INTRAVENOUS
DOSAGE FORM
SOLUTION
MARKETING STATUS
Prescription

Products

ZINC SULFATEPrescription
ZINC SULFATE EQ 10MG BASE/10ML (EQ 1MG BASE/ML) · SOLUTION · INTRAVENOUS
ZINC SULFATEPrescription
ZINC SULFATE EQ 25MG BASE/5ML (EQ 5MG BASE/ML) · SOLUTION · INTRAVENOUS

Approval history

2024-10-28Manufacturing (CMC) · Supplement 1 · unknownAP
2024-06-10UNKNOWN · 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 →