RABEPRAZOLE SODIUM
Summary
FDA approved RABEPRAZOLE SODIUM by TEVA PHARMS USA. ANDA (Generic) approval (Labeling) on 2021-09-14. TABLET, DELAYED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA076822-13
Action Date
2021-09-14
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
RABEPRAZOLE SODIUM, TABLET, DELAYED RELEASE, ORAL. Application: ANDA076822
Company
Context & Analysis
TEVA PHARMS USA has 39 FDA actions in our database.
Frequently Asked Questions
How often does TEVA PHARMS USA have FDA actions?
TEVA PHARMS USA has 39 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 "ANDA076822-13" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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