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General MedicationsORALGeneric

TIMOLIDE 10-25

HYDROCHLOROTHIAZIDE; TIMOLOL MALEATE

Standard Dose
25MG;10MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview TIMOLIDE 10-25 is listed in Drugs@FDA under application 018061 (NDA).

Marketing status: Discontinued Active ingredient HYDROCHLOROTHIAZIDE; TIMOLOL MALEATE Form and strength TABLET;ORAL - 25MG;10MG Sponsor MERCK Submission history Latest submission status date: 2009-03-13 00:00:00.

Structured Monograph

Clinical summary

Approval overview TIMOLIDE 10-25 is listed in Drugs@FDA under application 018061 (NDA). Marketing status: Discontinued Active ingredient HYDROCHLOROTHIAZIDE; TIMOLOL MALEATE Form and strength TABLET;ORAL - 25MG;10MG Sponsor MERCK Submission history Latest submission status date: 2009-03-13 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.