United States · FDA National Drug Code directory

GUNA-ANTI IL 1

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
17089-398_ed853c61-ca6e-4c3d-e053-2995a90aecb9
Product NDC
17089-398
Form
SOLUTION/ DROPS
Composition / generic term
ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT- CANAKINUMAB
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20080617
Source listing expiry
20261231

Source-listed ingredients

  • ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT — 4 [hp_C]/30mL
  • CANAKINUMAB — 4 [hp_C]/30mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, DROPPER in 1 BOX (17089-398-18) / 30 mL in 1 BOTTLE, DROPPER · 17089-398-18

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →