Drugplain

GUNA-ANTI IL 1 4 [hp_C]/30mL

ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT- CANAKINUMAB · SOLUTION/ DROPS · Guna spa

No Recall History
Plain English

GUNA-ANTI IL 1 is a solution/ drops containing anti-interleukin-1.alpha. immunoglobulin g rabbit- canakinumab at 4 [hp_C]/30mL, taken oral. Manufactured by Guna spa.

Key Facts

Brand Name
GUNA-ANTI IL 1
Generic Name
ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT- CANAKINUMAB
NDC Code (Product)
17089-398
Manufacturer
Guna spa
Strength
4 [hp_C]/30mL
Dosage Form
SOLUTION/ DROPS
Route
ORAL
Marketing Status
Marketing Start
06/17/2008

Recall History

No Recall History

Frequently Asked Questions

What is GUNA-ANTI IL 1 used for?

GUNA-ANTI IL 1 contains ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT- CANAKINUMAB. It is a solution/ drops taken oral. Consult your doctor for specific uses.

Is GUNA-ANTI IL 1 a controlled substance?

GUNA-ANTI IL 1 is not classified as a controlled substance by the DEA.

What is the generic name for GUNA-ANTI IL 1?

The generic name for GUNA-ANTI IL 1 is ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT- CANAKINUMAB. There are no other listed brand versions of ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT- CANAKINUMAB.

What is the NDC code for GUNA-ANTI IL 1 4 [hp_C]/30mL?

The NDC (National Drug Code) for GUNA-ANTI IL 1 4 [hp_C]/30mL is 17089-398, listed by Guna spa.

Product NDC

17089-398

Package NDC

17089-398-18

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

Data from openFDA · Public domain (CC0 1.0)