MORPHINE SULFATE
Summary
FDA approved MORPHINE SULFATE by SUN PHARM INDUSTRIES. ANDA (Generic) approval (REMS) on 2026-06-18. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA205634-10
Action Date
2026-06-18
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
MORPHINE SULFATE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA205634
Company
Context & Analysis
SUN PHARM INDUSTRIES has 19 FDA actions in our database.
Frequently Asked Questions
How often does SUN PHARM INDUSTRIES have FDA actions?
SUN PHARM INDUSTRIES has 19 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 "ANDA205634-10" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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