DEXMETHYLPHENIDATE HYDROCHLORIDE
Summary
FDA approved DEXMETHYLPHENIDATE HYDROCHLORIDE by SUN PHARM INDS INC. ANDA (Generic) approval (Labeling) on 2024-04-01. CAPSULE, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA206734-5
Action Date
2024-04-01
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
DEXMETHYLPHENIDATE HYDROCHLORIDE, CAPSULE, EXTENDED RELEASE, ORAL. Application: ANDA206734
Company
Context & Analysis
SUN PHARM INDS INC has 19 FDA actions in our database.
Frequently Asked Questions
How often does SUN PHARM INDS INC have FDA actions?
SUN PHARM INDS INC has 19 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 "ANDA206734-5" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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