TIZANIDINE HYDROCHLORIDE
Summary
FDA approved TIZANIDINE HYDROCHLORIDE by CADILA PHARMS LTD. ANDA (Generic) approval (Labeling) on 2022-05-25. CAPSULE, ORAL.
Details
Source
Drug Approval
External ID
ANDA210021-2
Action Date
2022-05-25
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
TIZANIDINE HYDROCHLORIDE, CAPSULE, ORAL. Application: ANDA210021
Company
Context & Analysis
CADILA PHARMS LTD has 9 FDA actions in our database.
Frequently Asked Questions
How often does CADILA PHARMS LTD have FDA actions?
CADILA PHARMS LTD has 9 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 "ANDA210021-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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