Guna-Inf Gamma (interferon gamma-1b) NDC 17089-378

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-378Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0378Add 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
17089-378-18	17089037818	1 BOTTLE, DROPPER in 1 BOX (17089-378-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Jun 17, 2008

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): Guna-Inf Gamma
Generic name (nonproprietary): interferon gamma-1b
Active ingredients: Interferon gamma-1b — 4 [hp_C]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 17, 2008
Listing expires: Dec 31, 2026
Other FDA classes: Interferon-gamma (Chemical structure)
Identifiers: Product ID 17089-378_ed813de7-e0d5-74b9-e053-2995a90a6a73SPL ID ed813de7-e0d5-74b9-e053-2995a90a6a73SPL set ID a09a33a1-5c7c-493d-abc7-907edd8e97caUNII 21K6M2I7AGUPC 0317089378181
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

N417089037818 followed by a unit qualifier and the quantity

Package 17089-0378-18. 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)