← FDA DRUG APPROVALS
FDA ANDA · ANDA090577
IMIPENEM AND CILASTATIN
imipenem and cilastatin sodium
Sponsor: ACS DOBFAR
APPLICATION
ANDA090577
TYPE
ANDA
ORIGINAL APPROVAL
2011-12-21
LATEST ACTION
2024-02-05
ROUTE
INTRAVENOUS
DOSAGE FORM
POWDER
MARKETING STATUS
Prescription
Products
IMIPENEM AND CILASTATINPrescription
CILASTATIN SODIUM EQ 500MG BASE/VIAL, IMIPENEM 500MG/VIAL · POWDER · INTRAVENOUS
IMIPENEM AND CILASTATINPrescription
CILASTATIN SODIUM EQ 250MG BASE/VIAL, IMIPENEM 250MG/VIAL · POWDER · INTRAVENOUS
Approval history
2024-02-05Labeling · Supplement 16 · standardAP
2019-07-09Labeling · Supplement 12 · standardAP
2019-07-09Labeling · Supplement 10 · standardAP
2015-05-29Labeling · Supplement 6 · standardAP
2015-05-29Labeling · Supplement 3 · standardAP
2015-04-15Labeling · Supplement 1AP
2011-12-21OriginalAP
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
Read a past issue →Get the Weekly GxP Briefing
Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.