RecallHawk

TERIPARATIDE

LILLY

Summary

FDA approved TERIPARATIDE by LILLY. NDA (New Drug) approval (Labeling) on 2024-07-24. SOLUTION, SUBCUTANEOUS.

Details

Source

Drug Approval

External ID

NDA021318-57

Action Date

2024-07-24

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

TERIPARATIDE, SOLUTION, SUBCUTANEOUS. Application: NDA021318

Company

Context & Analysis

LILLY has 6 FDA actions in our database.

Frequently Asked Questions

How often does LILLY have FDA actions?

LILLY 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 "NDA021318-57" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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