RecallHawk

SIGNIFOR LAR (PASIREOTIDE)

RECORDATI RARE

Summary

FDA approved SIGNIFOR LAR (PASIREOTIDE) by RECORDATI RARE. NDA (New Drug) approval (Labeling) on 2024-07-11. FOR SUSPENSION, INTRAMUSCULAR.

Details

Source

Drug Approval

External ID

NDA203255-11

Action Date

2024-07-11

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

SIGNIFOR LAR (generic: PASIREOTIDE), FOR SUSPENSION, INTRAMUSCULAR. Application: NDA203255

Context & Analysis

RECORDATI RARE has 2 FDA actions in our database.

Frequently Asked Questions

How often does RECORDATI RARE have FDA actions?

RECORDATI RARE 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 "NDA203255-11" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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