OXYMETAZOLINE HYDROCHLORIDE
Summary
FDA approved OXYMETAZOLINE HYDROCHLORIDE by SUN PHARMA CANADA. ANDA (Generic) approval on 2021-10-04. CREAM, TOPICAL.
Details
Source
Drug Approval
External ID
ANDA213584-1
Action Date
2021-10-04
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
OXYMETAZOLINE HYDROCHLORIDE, CREAM, TOPICAL. Application: ANDA213584
Company
Context & Analysis
SUN PHARMA CANADA has 10 FDA actions in our database.
Frequently Asked Questions
How often does SUN PHARMA CANADA have FDA actions?
SUN PHARMA CANADA has 10 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA213584-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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