ULTRA SLEEP AID (DOXYLAMINE SUCCINATE)
Summary
FDA approved ULTRA SLEEP AID (DOXYLAMINE SUCCINATE) by PERRIGO. ANDA (Generic) approval (Manufacturing (CMC)) on 2024-04-04. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA040167-52
Action Date
2024-04-04
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ULTRA SLEEP AID (generic: DOXYLAMINE SUCCINATE), TABLET, ORAL. Application: ANDA040167
Company
Context & Analysis
PERRIGO has 2 FDA actions in our database.
Frequently Asked Questions
How often does PERRIGO have FDA actions?
PERRIGO has 2 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 "ANDA040167-52" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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