Drugplain

EMGALITY 120 mg/mL

galcanezumab-gnlm · INJECTION, SOLUTION · Eli Lilly and Company

No Recall History
Plain English

EMGALITY is a injection, solution containing galcanezumab-gnlm at 120 mg/mL, taken subcutaneous. Manufactured by Eli Lilly and Company.

Key Facts

Brand Name
EMGALITY
Generic Name
galcanezumab-gnlm
NDC Code (Product)
0002-2377
Manufacturer
Eli Lilly and Company
Strength
120 mg/mL
Dosage Form
INJECTION, SOLUTION
Route
SUBCUTANEOUS
Marketing Status
Application #
BLA761063
Marketing Start
09/27/2018

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

injection site pain7,207 reports
migraine2,963 reports
underdose2,915 reports
headache2,384 reports
drug ineffective1,915 reports
product dose omission issue1,731 reports
injection site haemorrhage1,547 reports
injection site erythema1,111 reports
accidental underdose1,068 reports
incorrect dose administered953 reports

Frequently Asked Questions

What is EMGALITY used for?

EMGALITY contains galcanezumab-gnlm. It is a injection, solution taken subcutaneous. Consult your doctor for specific uses.

Is EMGALITY a controlled substance?

EMGALITY is not classified as a controlled substance by the DEA.

What is the generic name for EMGALITY?

The generic name for EMGALITY is galcanezumab-gnlm. There are no other listed brand versions of galcanezumab-gnlm.

What is the NDC code for EMGALITY 120 mg/mL?

The NDC (National Drug Code) for EMGALITY 120 mg/mL is 0002-2377, listed by Eli Lilly and Company.

Product NDC

0002-2377

Package NDC

0002-2377-11

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)