What is NDC 17089-259?

17089-259 is the product NDC for Osteobios, Calcitonin human 6 [hp_X]/30mL + 13 more ingredients 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?

Osteobios (Calcitonin human - calcium carbonate - calcium fluoride - calcium phosphate - isoleucine - leucine - lysine - methionine - phenylalanine - sus scrofa bone - sus scrofa parathyroid gland - threonine - tryptophan - valine -).

What is the active ingredient?

Calcitonin human, Isoleucine, Leucine, Lysine, Methionine, Phenylalanine, Threonine, Tryptophan, Valine, Calcium carbonate, Calcium fluoride, Calcium phosphate, Sus scrofa bone, Sus scrofa parathyroid gland.

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 Osteobios?

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.

Osteobios NDC 17089-259 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-259Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0259Add 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
17089-259-18	1708902591817089025918	1 BOTTLE, DROPPER in 1 BOX (17089-259-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from May 1, 2018

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): Osteobios
Generic name (nonproprietary): calcitonin human - calcium carbonate - calcium fluoride - calcium phosphate - isoleucine - leucine - lysine - methionine - phenylalanine - sus scrofa bone - sus scrofa parathyroid gland - threonine - tryptophan - valine -
Active ingredients: Calcitonin human — 6 [hp_X]/30mLIsoleucine — 3 [hp_X]/30mLLeucine — 3 [hp_X]/30mLLysine — 3 [hp_X]/30mLMethionine — 3 [hp_X]/30mLPhenylalanine — 3 [hp_X]/30mLThreonine — 3 [hp_X]/30mLTryptophan — 3 [hp_X]/30mLValine — 3 [hp_X]/30mLCalcium carbonate — 30 [hp_X]/30mLCalcium fluoride — 30 [hp_X]/30mLCalcium phosphate — 30 [hp_X]/30mLSus scrofa bone — 30 [hp_X]/30mLSus scrofa parathyroid gland — 30 [hp_X]/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: May 23, 2006
Listing expires: Dec 31, 2027
Other FDA classes: Calcium (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Coagulation Factor Activity (Physiologic effect)
Identifiers: Product ID 17089-259_ed712a71-07a8-02bc-e053-2995a90a8c42SPL ID ed712a71-07a8-02bc-e053-2995a90a8c42SPL set ID 1b8c8c83-1a46-4c0a-b883-e7dce781c5d1UNII I0IO929019, 04Y7590D77, GMW67QNF9C, K3Z4F929H6, AE28F7PNPL, 47E5O17Y3R, 2ZD004190S, 8DUH1N11BX, HG18B9YRS7, H0G9379FGK, O3B55K4YKI, 97Z1WI3NDX, 597RLJ09RG, 2KBE35NE8SUPC 0317089259183
Pharmacologic class: Blood Coagulation Factor

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

N417089025918 followed by a unit qualifier and the quantity

Package 17089-0259-18. 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 14, 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 17089-259

What is NDC 17089-259?: 17089-259 is the product NDC for Osteobios, Calcitonin human 6 [hp_X]/30mL + 13 more ingredients 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?: Osteobios (Calcitonin human - calcium carbonate - calcium fluoride - calcium phosphate - isoleucine - leucine - lysine - methionine - phenylalanine - sus scrofa bone - sus scrofa parathyroid gland - threonine - tryptophan - valine -).
What is the active ingredient?: Calcitonin human, Isoleucine, Leucine, Lysine, Methionine, Phenylalanine, Threonine, Tryptophan, Valine, Calcium carbonate, Calcium fluoride, Calcium phosphate, Sus scrofa bone, Sus scrofa parathyroid gland.
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 Osteobios?: 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.