DILTIAZEM HYDROCHLORIDE
Summary
FDA approved DILTIAZEM HYDROCHLORIDE by SCIEGEN PHARMS. ANDA (Generic) approval on 2022-09-23. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA216521-1
Action Date
2022-09-23
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
DILTIAZEM HYDROCHLORIDE, TABLET, ORAL. Application: ANDA216521
Company
Context & Analysis
SCIEGEN PHARMS has 20 FDA actions in our database.
Frequently Asked Questions
How often does SCIEGEN PHARMS have FDA actions?
SCIEGEN PHARMS has 20 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 "ANDA216521-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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