What is NDC 17089-405?

17089-405 is the product NDC for Gamma -12, Interferon gamma-1b 4 [hp_C]/30mL; Interleukin-12 human recombinant 4 [hp_C]/30mL solution/ drops, listed with the FDA by Guna spa. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Gamma -12 (Interleukin-12 human recombinant - interferon gamma-1b -).

What is the active ingredient?

Interferon gamma-1b, Interleukin-12 human recombinant.

Guna spa, NDC labeler code 17089. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Gamma -12?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Gamma -12 NDC 17089-405 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-405Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0405Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
17089-405-18	17089040518	1 BOTTLE, DROPPER in 1 BOX (17089-405-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Mar 31, 2011

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Gamma -12
Generic name (nonproprietary): interleukin-12 human recombinant - interferon gamma-1b -
Active ingredients: Interferon gamma-1b — 4 [hp_C]/30mLInterleukin-12 human recombinant — 4 [hp_C]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spaNDC labeler code 17089
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 29, 2010
Listing expires: Dec 31, 2026
Other FDA classes: Interferon-gamma (Chemical structure)
Identifiers: Product ID 17089-405_ed853c61-ca74-4c3d-e053-2995a90aecb9SPL ID ed853c61-ca74-4c3d-e053-2995a90aecb9SPL set ID c3366fcd-7d7a-4cf8-995c-798b6d2c9ad1UNII 21K6M2I7AG, 02FXP10O2U
Pharmacologic class: Interferon gamma

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N417089040518 followed by a unit qualifier and the quantity

Package 17089-0405-18. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Nov 15, 2022.

Indications (excerpt from the label)

take 15 minutes before meals

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17089-405

What is NDC 17089-405?: 17089-405 is the product NDC for Gamma -12, Interferon gamma-1b 4 [hp_C]/30mL; Interleukin-12 human recombinant 4 [hp_C]/30mL solution/ drops, listed with the FDA by Guna spa. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Gamma -12 (Interleukin-12 human recombinant - interferon gamma-1b -).
What is the active ingredient?: Interferon gamma-1b, Interleukin-12 human recombinant.
Who is the labeler?: Guna spa, NDC labeler code 17089. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Gamma -12?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.