ATROPINE SULFATE
Summary
FDA approved ATROPINE SULFATE by HIKMA. ANDA (Generic) approval on 2021-12-01. SOLUTION, INTRAVENOUS, INTRAMUSCULAR, SUBCUTANEOUS, INTRAOSSEOUS, ENDOTRACHEAL.
Details
Source
Drug Approval
External ID
ANDA213561-1
Action Date
2021-12-01
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ATROPINE SULFATE, SOLUTION, INTRAVENOUS, INTRAMUSCULAR, SUBCUTANEOUS, INTRAOSSEOUS, ENDOTRACHEAL. Application: ANDA213561
Company
Context & Analysis
HIKMA has 117 FDA actions in our database.
Frequently Asked Questions
How often does HIKMA have FDA actions?
HIKMA has 117 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 "ANDA213561-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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