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General MedicationsOPHTHALMICGeneric

CYCLOPENTOLATE HYDROCHLORIDE

CYCLOPENTOLATE HYDROCHLORIDE

Standard Dose
1%
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview CYCLOPENTOLATE HYDROCHLORIDE is listed in Drugs@FDA under application 089162 (ANDA).

Marketing status: Discontinued Active ingredient CYCLOPENTOLATE HYDROCHLORIDE Form and strength SOLUTION/DROPS;OPHTHALMIC - 1% Sponsor ALCON PHARMS LTD Submission history Latest submission status date: 1996-06-07 00:00:00.

Structured Monograph

Clinical summary

Approval overview CYCLOPENTOLATE HYDROCHLORIDE is listed in Drugs@FDA under application 089162 (ANDA). Marketing status: Discontinued Active ingredient CYCLOPENTOLATE HYDROCHLORIDE Form and strength SOLUTION/DROPS;OPHTHALMIC - 1% Sponsor ALCON PHARMS LTD Submission history Latest submission status date: 1996-06-07 00:00:00. Submission type: SUPPL.

Monitoring

  • • Review priority: STANDARD
  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.