United States · FDA National Drug Code directory
GAMMA -12
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
- 17089-405_ed853c61-ca74-4c3d-e053-2995a90aecb9
- Product NDC
- 17089-405
- Form
- SOLUTION/ DROPS
- Composition / generic term
- INTERLEUKIN-12 HUMAN RECOMBINANT - INTERFERON GAMMA-1B -
- Labeler
- Guna spa
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20100429
- Source listing expiry
- 20261231
Source-listed ingredients
- INTERFERON GAMMA-1B — 4 [hp_C]/30mL
- INTERLEUKIN-12 HUMAN RECOMBINANT — 4 [hp_C]/30mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, DROPPER in 1 BOX (17089-405-18) / 30 mL in 1 BOTTLE, DROPPER · 17089-405-18
Source and coverage
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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.
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