RecallHawk

IMIPENEM AND CILASTATIN (IMIPENEM AND CILASTATIN SODIUM)

ACS DOBFAR

Summary

FDA approved IMIPENEM AND CILASTATIN (IMIPENEM AND CILASTATIN SODIUM) by ACS DOBFAR. ANDA (Generic) approval (Labeling) on 2024-02-05. POWDER, INTRAVENOUS.

Details

Source

Drug Approval

External ID

ANDA090577-16

Action Date

2024-02-05

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

IMIPENEM AND CILASTATIN (generic: IMIPENEM AND CILASTATIN SODIUM), POWDER, INTRAVENOUS. Application: ANDA090577

Company

Context & Analysis

ACS DOBFAR has 2 FDA actions in our database.

Frequently Asked Questions

How often does ACS DOBFAR have FDA actions?

ACS DOBFAR has 2 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 "ANDA090577-16" 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