GALANTAMINE HYDROBROMIDE
Summary
FDA approved GALANTAMINE HYDROBROMIDE by APOTEX INC. ANDA (Generic) approval (Labeling) on 2023-06-28. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA077781-10
Action Date
2023-06-28
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
GALANTAMINE HYDROBROMIDE, TABLET, ORAL. Application: ANDA077781
Company
Context & Analysis
APOTEX INC has 17 FDA actions in our database.
Frequently Asked Questions
How often does APOTEX INC have FDA actions?
APOTEX INC has 17 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 "ANDA077781-10" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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