RecallHawk

VARENICLINE TARTRATE

VIWIT PHARM

Summary

FDA approved VARENICLINE TARTRATE by VIWIT PHARM. ANDA (Generic) approval on 2025-05-06. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA212879-1

Action Date

2025-05-06

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

VARENICLINE TARTRATE, TABLET, ORAL. Application: ANDA212879

Context & Analysis

VIWIT PHARM has 5 FDA actions in our database.

Frequently Asked Questions

How often does VIWIT PHARM have FDA actions?

VIWIT PHARM has 5 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 "ANDA212879-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for drug

Related Actions