RecallHawk

LANSOPRAZOLE

XIROMED

Summary

FDA approved LANSOPRAZOLE by XIROMED. ANDA (Generic) approval (Labeling) on 2023-04-06. CAPSULE, DELAYED REL PELLETS, ORAL.

Details

Source

Drug Approval

External ID

ANDA203203-11

Action Date

2023-04-06

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

LANSOPRAZOLE, CAPSULE, DELAYED REL PELLETS, ORAL. Application: ANDA203203

Company

Context & Analysis

XIROMED has 23 FDA actions in our database.

Frequently Asked Questions

How often does XIROMED have FDA actions?

XIROMED has 23 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 "ANDA203203-11" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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