RecallHawk

Summary

FDA approved MEROPENEM by HQ SPCLT PHARMA. NDA (New Drug) approval (Labeling) on 2024-12-03. POWDER, INTRAVENOUS.

Details

Source

Drug Approval

External ID

NDA215212-2

Action Date

2024-12-03

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

MEROPENEM, POWDER, INTRAVENOUS. Application: NDA215212

Context & Analysis

HQ SPCLT PHARMA has 6 FDA actions in our database.

Frequently Asked Questions

How often does HQ SPCLT PHARMA have FDA actions?

HQ SPCLT PHARMA has 6 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 "NDA215212-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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