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DUAL ACTION (ACETAMINOPHEN, IBUPROFEN)

MARKSANS PHARMA

Summary

FDA approved DUAL ACTION (ACETAMINOPHEN, IBUPROFEN) by MARKSANS PHARMA. ANDA (Generic) approval on 2023-07-10. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA216994-1

Action Date

2023-07-10

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

DUAL ACTION (generic: ACETAMINOPHEN, IBUPROFEN), TABLET, ORAL. Application: ANDA216994

Context & Analysis

MARKSANS PHARMA has 8 FDA actions in our database.

Frequently Asked Questions

How often does MARKSANS PHARMA have FDA actions?

MARKSANS PHARMA has 8 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 "ANDA216994-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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