NIFEDIPINE
Summary
FDA approved NIFEDIPINE by NOVAST LABS. ANDA (Generic) approval (Labeling) on 2023-05-01. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA202987-3
Action Date
2023-05-01
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
NIFEDIPINE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA202987
Company
Context & Analysis
NOVAST LABS has 14 FDA actions in our database.
Frequently Asked Questions
How often does NOVAST LABS have FDA actions?
NOVAST LABS has 14 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 "ANDA202987-3" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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