General MedicationsTOPICALGeneric
OXYMETAZOLINE HYDROCHLORIDE
OXYMETAZOLINE HYDROCHLORIDE
Standard Dose
1%
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary
Approval overview OXYMETAZOLINE HYDROCHLORIDE is listed in Drugs@FDA under application 213584 (ANDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient OXYMETAZOLINE HYDROCHLORIDE Form and strength CREAM;TOPICAL - 1% Sponsor SUN PHARMA CANADA Submission history Latest submission status date: 2021-10-04 00:00:00.
Structured Monograph
Clinical summary
Approval overview OXYMETAZOLINE HYDROCHLORIDE is listed in Drugs@FDA under application 213584 (ANDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient OXYMETAZOLINE HYDROCHLORIDE Form and strength CREAM;TOPICAL - 1% Sponsor SUN PHARMA CANADA Submission history Latest submission status date: 2021-10-04 00:00:00. Submission type: ORIG.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.