← FDA DRUG APPROVALS

FDA ANDA · ANDA065421

RIFAMPIN

Sponsor: MYLAN LABS LTD

APPLICATION
ANDA065421
TYPE
ANDA
ORIGINAL APPROVAL
2008-05-22
LATEST ACTION
2025-04-03
ROUTE
INTRAVENOUS, INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Prescription

Products

RIFAMPINPrescription
RIFAMPIN 600MG/VIAL · INJECTABLE · INJECTION

Approval history

2025-04-03Labeling · Supplement 29 · standardAP
2024-02-15Labeling · Supplement 19 · standardAP
2024-02-15Labeling · Supplement 23 · standardAP
2024-02-15Labeling · Supplement 21 · standardAP
2024-02-15Labeling · Supplement 26 · standardAP
2024-02-15Labeling · Supplement 18 · standardAP
2020-07-01Labeling · Supplement 9 · standardAP
2020-07-01Labeling · Supplement 8 · standardAP
2020-07-01Labeling · Supplement 14 · standardAP
2015-10-27Labeling · Supplement 3 · standardAP
2008-05-22OriginalAP
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 →