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FDA ANDA · ANDA062720

CEPHAPIRIN SODIUM

Sponsor: HIKMA

APPLICATION
ANDA062720
TYPE
ANDA
ORIGINAL APPROVAL
1987-07-02
LATEST ACTION
1987-07-02
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued

Products

CEPHAPIRIN SODIUMDiscontinued
CEPHAPIRIN SODIUM EQ 20GM BASE/VIAL · INJECTABLE · INJECTION
CEPHAPIRIN SODIUMDiscontinued
CEPHAPIRIN SODIUM EQ 1GM BASE/VIAL · INJECTABLE · INJECTION
CEPHAPIRIN SODIUMDiscontinued
CEPHAPIRIN SODIUM EQ 2GM BASE/VIAL · INJECTABLE · INJECTION
CEPHAPIRIN SODIUMDiscontinued
CEPHAPIRIN SODIUM EQ 500MG BASE/VIAL · INJECTABLE · INJECTION

Approval history

1987-07-02OriginalAP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

Pharma industry →GMP discipline →FDA drug shortages →FDA 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.

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