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General MedicationsORALGeneric

IBANDRONATE SODIUM

IBANDRONATE SODIUM

Standard Dose
2.5MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: None (Tentative Approval)
Summary

Approval overview IBANDRONATE SODIUM is listed in Drugs@FDA under application 079002 (ANDA).

Marketing status: None (Tentative Approval) Active ingredient IBANDRONATE SODIUM Form and strength TABLET; ORAL - 2.5MG Sponsor COBALT LABS INC Submission history Latest submission status date: 2011-03-15 00:00:00.

Structured Monograph

Clinical summary

Approval overview IBANDRONATE SODIUM is listed in Drugs@FDA under application 079002 (ANDA). Marketing status: None (Tentative Approval) Active ingredient IBANDRONATE SODIUM Form and strength TABLET; ORAL - 2.5MG Sponsor COBALT LABS INC Submission history Latest submission status date: 2011-03-15 00:00:00. Submission type: ORIG.

Monitoring

  • • Marketing status: None (Tentative Approval)

Interaction Notes

  • No interaction notes stored yet.