THEOPHYLLINE
Summary
FDA approved THEOPHYLLINE by TEVA PHARMS INC. ANDA (Generic) approval on 2022-10-12. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA216961-1
Action Date
2022-10-12
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
THEOPHYLLINE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA216961
Company
Context & Analysis
TEVA PHARMS INC has 7 FDA actions in our database.
Frequently Asked Questions
How often does TEVA PHARMS INC have FDA actions?
TEVA PHARMS INC has 7 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 "ANDA216961-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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