RecallHawk

OLANZAPINE

ASPIRO

Summary

FDA approved OLANZAPINE by ASPIRO. ANDA (Generic) approval on 2023-03-22. POWDER, INTRAMUSCULAR.

Details

Source

Drug Approval

External ID

ANDA217466-1

Action Date

2023-03-22

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

OLANZAPINE, POWDER, INTRAMUSCULAR. Application: ANDA217466

Company

Context & Analysis

ASPIRO has 12 FDA actions in our database.

Frequently Asked Questions

How often does ASPIRO have FDA actions?

ASPIRO has 12 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 "ANDA217466-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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