NEBIVOLOL HYDROCHLORIDE
Summary
FDA approved NEBIVOLOL HYDROCHLORIDE by REYOUNG. ANDA (Generic) approval on 2021-12-17. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA212917-1
Action Date
2021-12-17
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
NEBIVOLOL HYDROCHLORIDE, TABLET, ORAL. Application: ANDA212917
Company
Context & Analysis
Frequently Asked Questions
How often does REYOUNG have FDA actions?
This is the only FDA action we have on record for REYOUNG in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA212917-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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