NALMEFENE HYDROCHLORIDE (NALMEFENE HYDROCHLORIDE INJECTION)
Summary
FDA approved NALMEFENE HYDROCHLORIDE (NALMEFENE HYDROCHLORIDE INJECTION) by CHENGDU SHUODE. ANDA (Generic) approval on 2023-11-15. SOLUTION, INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS.
Details
Source
Drug Approval
External ID
ANDA216007-1
Action Date
2023-11-15
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
NALMEFENE HYDROCHLORIDE (generic: NALMEFENE HYDROCHLORIDE INJECTION), SOLUTION, INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS. Application: ANDA216007
Company
Context & Analysis
Frequently Asked Questions
How often does CHENGDU SHUODE have FDA actions?
This is the only FDA action we have on record for CHENGDU SHUODE in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA216007-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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