AZULFIDINE EN-TABS (SULFASALAZINE)
Summary
FDA approved AZULFIDINE EN-TABS (SULFASALAZINE) by PFIZER. NDA (New Drug) approval (Labeling) on 2022-11-16. TABLET, DELAYED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
NDA007073-133
Action Date
2022-11-16
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
AZULFIDINE EN-TABS (generic: SULFASALAZINE), TABLET, DELAYED RELEASE, ORAL. Application: NDA007073
Company
Context & Analysis
PFIZER has 28 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
How often does PFIZER have FDA actions?
PFIZER has 28 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA007073-133" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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