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General MedicationsINJECTIONStandard

MYCOPHENOLATE MOFETIL HYDROCHLORIDE

MYCOPHENOLATE MOFETIL HYDROCHLORIDE

Standard Dose
500MG/VIAL
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Prescription
Summary

Approval overview MYCOPHENOLATE MOFETIL HYDROCHLORIDE is listed in Drugs@FDA under application 216390 (ANDA).

Marketing status: Prescription Active ingredient MYCOPHENOLATE MOFETIL HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - 500MG/VIAL Sponsor ONESOURCE SPECIALTY Submission history Latest submission status date: 2024-08-13 00:00:00.

Structured Monograph

Clinical summary

Approval overview MYCOPHENOLATE MOFETIL HYDROCHLORIDE is listed in Drugs@FDA under application 216390 (ANDA). Marketing status: Prescription Active ingredient MYCOPHENOLATE MOFETIL HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - 500MG/VIAL Sponsor ONESOURCE SPECIALTY Submission history Latest submission status date: 2024-08-13 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.