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General MedicationsINTRAVENOUSStandard

ULTRA-TECHNEKOW V4

TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR

Standard Dose
1-19 CI/GENERATOR
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Prescription
Summary

Approval overview ULTRA-TECHNEKOW V4 is listed in Drugs@FDA under application 017243 (NDA).

Review priority: STANDARD Marketing status: Prescription Active ingredient TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR Form and strength SOLUTION;INTRAVENOUS - 1-19 CI/GENERATOR Sponsor CURIUM Submission history Latest submission status date: 2017-01-30 00:00:00.

Structured Monograph

Clinical summary

Approval overview ULTRA-TECHNEKOW V4 is listed in Drugs@FDA under application 017243 (NDA). Review priority: STANDARD Marketing status: Prescription Active ingredient TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR Form and strength SOLUTION;INTRAVENOUS - 1-19 CI/GENERATOR Sponsor CURIUM Submission history Latest submission status date: 2017-01-30 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Prescription
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.
ULTRA-TECHNEKOW V4 (TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR) | Drug Monograph | MedicHelpline