CLONIDINE HYDROCHLORIDE
Summary
FDA approved CLONIDINE HYDROCHLORIDE by XIAMEN LP PHARM CO. ANDA (Generic) approval (Labeling) on 2023-07-10. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA209757-2
Action Date
2023-07-10
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
CLONIDINE HYDROCHLORIDE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA209757
Company
Context & Analysis
XIAMEN LP PHARM CO has 5 FDA actions in our database.
Frequently Asked Questions
How often does XIAMEN LP PHARM CO have FDA actions?
XIAMEN LP PHARM CO has 5 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 "ANDA209757-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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