General MedicationsINTRAVENOUSGeneric
OXACILLIN SODIUM
OXACILLIN SODIUM
Standard Dose
EQ 1GM BASE/VIAL
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary
Approval overview OXACILLIN SODIUM is listed in Drugs@FDA under application 062737 (ANDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient OXACILLIN SODIUM Form and strength POWDER;INTRAVENOUS - EQ 1GM BASE/VIAL Sponsor SANDOZ Submission history Latest submission status date: 2016-05-25 00:00:00.
Structured Monograph
Clinical summary
Approval overview OXACILLIN SODIUM is listed in Drugs@FDA under application 062737 (ANDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient OXACILLIN SODIUM Form and strength POWDER;INTRAVENOUS - EQ 1GM BASE/VIAL Sponsor SANDOZ Submission history Latest submission status date: 2016-05-25 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.