SUTAB
MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM SULFATE
Approval overview SUTAB is listed in Drugs@FDA under application 213135 (NDA).
Review priority: STANDARD Marketing status: Prescription Active ingredient MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM SULFATE Form and strength TABLET;ORAL - 0.225GM;0.188GM;1.479GM Sponsor AZURITY Submission history Latest submission status date: 2023-10-24 00:00:00.
Structured Monograph
Clinical summary
Approval overview SUTAB is listed in Drugs@FDA under application 213135 (NDA). Review priority: STANDARD Marketing status: Prescription Active ingredient MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM SULFATE Form and strength TABLET;ORAL - 0.225GM;0.188GM;1.479GM Sponsor AZURITY Submission history Latest submission status date: 2023-10-24 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Prescription
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.