HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Summary
FDA approved HYDROCODONE BITARTRATE AND ACETAMINOPHEN by ACTAVIS LABS FL INC. ANDA (Generic) approval (REMS) on 2026-06-18. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA206470-17
Action Date
2026-06-18
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
HYDROCODONE BITARTRATE AND ACETAMINOPHEN, TABLET, ORAL. Application: ANDA206470
Company
Context & Analysis
ACTAVIS LABS FL INC has 17 FDA actions in our database.
Frequently Asked Questions
How often does ACTAVIS LABS FL INC have FDA actions?
ACTAVIS LABS FL 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 "ANDA206470-17" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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