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General MedicationsORALGeneric

PROCAINAMIDE HYDROCHLORIDE

PROCAINAMIDE HYDROCHLORIDE

Standard Dose
750MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview PROCAINAMIDE HYDROCHLORIDE is listed in Drugs@FDA under application 089438 (ANDA).

Marketing status: Discontinued Active ingredient PROCAINAMIDE HYDROCHLORIDE Form and strength TABLET, EXTENDED RELEASE;ORAL - 750MG Sponsor ANI PHARMS Submission history Latest submission status date: 2002-12-09 00:00:00.

Structured Monograph

Clinical summary

Approval overview PROCAINAMIDE HYDROCHLORIDE is listed in Drugs@FDA under application 089438 (ANDA). Marketing status: Discontinued Active ingredient PROCAINAMIDE HYDROCHLORIDE Form and strength TABLET, EXTENDED RELEASE;ORAL - 750MG Sponsor ANI PHARMS Submission history Latest submission status date: 2002-12-09 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.