ACETYLCYSTEINE
Summary
FDA approved ACETYLCYSTEINE by EXELA PHARMA. ANDA (Generic) approval on 2023-11-01. SOLUTION, INHALATION, ORAL.
Details
Source
Drug Approval
External ID
ANDA205643-1
Action Date
2023-11-01
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ACETYLCYSTEINE, SOLUTION, INHALATION, ORAL. Application: ANDA205643
Company
Context & Analysis
EXELA PHARMA has 5 FDA actions in our database.
Frequently Asked Questions
How often does EXELA PHARMA have FDA actions?
EXELA PHARMA has 5 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 "ANDA205643-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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