MUCINEX (GUAIFENESIN)
Summary
FDA approved MUCINEX (GUAIFENESIN) by RB HLTH. NDA (New Drug) approval (Labeling) on 2024-08-30. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
NDA021282-55
Action Date
2024-08-30
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
MUCINEX (generic: GUAIFENESIN), TABLET, EXTENDED RELEASE, ORAL. Application: NDA021282
Company
Context & Analysis
RB HLTH has 4 FDA actions in our database.
Frequently Asked Questions
How often does RB HLTH have FDA actions?
RB HLTH has 4 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 "NDA021282-55" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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