ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE
Summary
FDA approved ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE by TARO PHARM INDS. ANDA (Generic) approval (Labeling) on 2022-05-27. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA075788-21
Action Date
2022-05-27
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE, TABLET, ORAL. Application: ANDA075788
Company
Context & Analysis
TARO PHARM INDS has 2 FDA actions in our database.
Frequently Asked Questions
How often does TARO PHARM INDS have FDA actions?
TARO PHARM INDS has 2 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 "ANDA075788-21" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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