RecallHawk

ONDANSETRON HYDROCHLORIDE

APOTEX INC

Summary

FDA approved ONDANSETRON HYDROCHLORIDE by APOTEX INC. ANDA (Generic) approval (Labeling) on 2022-03-15. INJECTABLE, INJECTION.

Details

Source

Drug Approval

External ID

ANDA077368-10

Action Date

2022-03-15

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

ONDANSETRON HYDROCHLORIDE, INJECTABLE, INJECTION. Application: ANDA077368

Company

Context & Analysis

APOTEX INC has 17 FDA actions in our database.

Frequently Asked Questions

How often does APOTEX INC have FDA actions?

APOTEX INC has 17 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 "ANDA077368-10" 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