HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO)
Summary
FDA approved HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO) by LILLY. BLA (Biologic) approval (Labeling) on 2023-07-21. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
BLA021018-132
Action Date
2023-07-21
Status
Approved
Category
drug
Product Code
BLA (Biologic)
Product Description
HUMALOG MIX50/50 KWIKPEN (generic: INSULIN LISPRO), INJECTABLE, INJECTION. Application: BLA021018
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 "BLA021018-132" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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