EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE
Summary
FDA approved EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE by HETERO LABS LTD III. ANDA (Generic) approval (Not Applicable) on 2021-10-07. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA201806-1
Action Date
2021-10-07
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE, TABLET, ORAL. Application: ANDA201806
Company
Context & Analysis
HETERO LABS LTD III has 21 FDA actions in our database.
Frequently Asked Questions
How often does HETERO LABS LTD III have FDA actions?
HETERO LABS LTD III has 21 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 "ANDA201806-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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