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General MedicationsINJECTIONGeneric

DUOCAINE

BUPIVACAINE HYDROCHLORIDE; LIDOCAINE HYDROCHLORIDE

Standard Dose
EQ 0.375% (37.5MG/10ML);EQ 1% (100MG/10ML)
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview DUOCAINE is listed in Drugs@FDA under application 021496 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient BUPIVACAINE HYDROCHLORIDE; LIDOCAINE HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - EQ 0.375% (37.5MG/10ML);EQ 1% (100MG/10ML) Sponsor AMPHASTAR PHARMS INC Submission history Latest submission status date: 2003-05-23 00:00:00.

Structured Monograph

Clinical summary

Approval overview DUOCAINE is listed in Drugs@FDA under application 021496 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient BUPIVACAINE HYDROCHLORIDE; LIDOCAINE HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - EQ 0.375% (37.5MG/10ML);EQ 1% (100MG/10ML) Sponsor AMPHASTAR PHARMS INC Submission history Latest submission status date: 2003-05-23 00:00:00. Submission type: ORIG.

Monitoring

  • Marketing status: Discontinued
  • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.
DUOCAINE (BUPIVACAINE HYDROCHLORIDE; LIDOCAINE HYDROCHLORIDE) | Drug Monograph | MedicHelpline