DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE
Summary
FDA approved DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE by NUVO PHARM. ANDA (Generic) approval (Labeling) on 2023-10-13. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA209799-4
Action Date
2023-10-13
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE, TABLET, ORAL. Application: ANDA209799
Company
Context & Analysis
NUVO PHARM has 3 FDA actions in our database.
Frequently Asked Questions
How often does NUVO PHARM have FDA actions?
NUVO PHARM has 3 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 "ANDA209799-4" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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