TRIENTINE HYDROCHLORIDE
Summary
FDA approved TRIENTINE HYDROCHLORIDE by DR REDDYS. ANDA (Generic) approval (Labeling) on 2025-04-09. CAPSULE, ORAL.
Details
Source
Drug Approval
External ID
ANDA211076-6
Action Date
2025-04-09
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
TRIENTINE HYDROCHLORIDE, CAPSULE, ORAL. Application: ANDA211076
Company
Context & Analysis
DR REDDYS has 47 FDA actions in our database.
Frequently Asked Questions
How often does DR REDDYS have FDA actions?
DR REDDYS has 47 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 "ANDA211076-6" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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