General MedicationsINJECTIONGeneric
CEFOTAXIME
CEFOTAXIME SODIUM
Standard Dose
EQ 20GM BASE/VIAL
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary
Approval overview CEFOTAXIME is listed in Drugs@FDA under application 064201 (ANDA).
Marketing status: Discontinued Active ingredient CEFOTAXIME SODIUM Form and strength INJECTABLE;INJECTION - EQ 20GM BASE/VIAL Sponsor FRESENIUS KABI USA Submission history Latest submission status date: 2008-04-30 00:00:00.
Structured Monograph
Clinical summary
Approval overview CEFOTAXIME is listed in Drugs@FDA under application 064201 (ANDA). Marketing status: Discontinued Active ingredient CEFOTAXIME SODIUM Form and strength INJECTABLE;INJECTION - EQ 20GM BASE/VIAL Sponsor FRESENIUS KABI USA Submission history Latest submission status date: 2008-04-30 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
Interaction Notes
- No interaction notes stored yet.