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General MedicationsINJECTIONGeneric

MYCOPHENOLATE MOFETIL HYDROCHLORIDE

MYCOPHENOLATE MOFETIL HYDROCHLORIDE

Standard Dose
500MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: None (Tentative Approval)
Summary

Approval overview MYCOPHENOLATE MOFETIL HYDROCHLORIDE is listed in Drugs@FDA under application 090311 (ANDA).

Marketing status: None (Tentative Approval) Active ingredient MYCOPHENOLATE MOFETIL HYDROCHLORIDE Form and strength INJECTABLE; INJECTION - 500MG Sponsor BEDFORD LABS Submission history Latest submission status date: 2010-09-30 00:00:00.

Structured Monograph

Clinical summary

Approval overview MYCOPHENOLATE MOFETIL HYDROCHLORIDE is listed in Drugs@FDA under application 090311 (ANDA). Marketing status: None (Tentative Approval) Active ingredient MYCOPHENOLATE MOFETIL HYDROCHLORIDE Form and strength INJECTABLE; INJECTION - 500MG Sponsor BEDFORD LABS Submission history Latest submission status date: 2010-09-30 00:00:00. Submission type: ORIG.

Monitoring

  • • Marketing status: None (Tentative Approval)

Interaction Notes

  • No interaction notes stored yet.