PROTONIX I.V. (PANTOPRAZOLE SODIUM)
Summary
FDA approved PROTONIX I.V. (PANTOPRAZOLE SODIUM) by WYETH PHARMS. NDA (New Drug) approval (Efficacy) on 2024-08-12. INJECTABLE, INTRAVENOUS.
Details
Source
Drug Approval
External ID
NDA020988-70
Action Date
2024-08-12
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
PROTONIX I.V. (generic: PANTOPRAZOLE SODIUM), INJECTABLE, INTRAVENOUS. Application: NDA020988
Company
Context & Analysis
WYETH PHARMS has 4 FDA actions in our database.
Frequently Asked Questions
How often does WYETH PHARMS have FDA actions?
WYETH PHARMS 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 "NDA020988-70" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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