What is NDC 85477-902?

85477-902 is the product NDC for Folixia (multivitamin), Ferrous bisglycinate 20 mg/1 + 11 more ingredients tablet, listed with the FDA by Oncora Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Ferrous bisglycinate, Potassium iodide, Pyridoxine hydrochloride, Beta carotene, Ascorbic acid, Cholecalciferol, Biotin, Folic acid, Cyanocobalamin, Calcium carbonate, Magnesium oxide, .alpha.-tocopherol acetate, Dl-.

Oncora Pharma, LLC, NDC labeler code 85477. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Folixia?

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.

Folixia NDC 85477-902 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)85477-902Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85477-0902Add 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
85477-902-30	8547709023085477090230	30 TABLET in 1 BOTTLE (85477-902-30)Marketed from Feb 24, 2025

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): Folixia
Generic name (nonproprietary): multivitamin
Active ingredients: Ferrous bisglycinate — 20 mg/1Potassium iodide — .15 mg/1Pyridoxine hydrochloride — 26 mg/1Beta carotene — .3 mg/1Ascorbic acid — 60 mg/1Cholecalciferol — .1 mg/1Biotin — .28 mg/1Folic acid — 1.67 mg/1Cyanocobalamin — .013 mg/1Calcium carbonate — 80 mg/1Magnesium oxide — 25 mg/1.alpha.-tocopherol acetate, Dl- — 4.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Oncora Pharma, LLCNDC labeler code 85477
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Feb 24, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Analogs/Derivatives (Chemical/Ingredient)Ascorbic Acid (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)Vitamin B 12 (Chemical structure)Vitamin B 6 (Chemical/Ingredient)Vitamin D (Chemical structure)
Identifiers: Product ID 85477-902_4aa3e0fa-38cd-3f45-e063-6394a90a9a2bSPL ID 4aa3e0fa-38cd-3f45-e063-6394a90a9a2bSPL set ID 413945b5-116b-d8b6-e063-6394a90a55e8UNII SFW1D987QV, 1C4QK22F9J, 68Y4CF58BV, 01YAE03M7J, PQ6CK8PD0R, 1C6V77QF41, 6SO6U10H04, 935E97BOY8, P6YC3EG204, H0G9379FGK, 3A3U0GI71G, WR1WPI7EW8
Pharmacologic class: Blood Coagulation Factor; Calculi Dissolution Agent; Osmotic Laxative; Phosphate Binder; Vitamin B12; Vitamin B6 Analog; Vitamin C; Vitamin D

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

N485477090230 followed by a unit qualifier and the quantity

Package 85477-0902-30. 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 Feb 12, 2026.

Indications (excerpt from the label)

Folixia is a prescription multivitamin/multi-mineral dietary supplement formulated for the clinical dietary management of a subuoptimal nutritional status in patients where advanced folate, vitamin B supplementation, and maintenance of good health is needed.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85477-902

What is NDC 85477-902?: 85477-902 is the product NDC for Folixia (multivitamin), Ferrous bisglycinate 20 mg/1 + 11 more ingredients tablet, listed with the FDA by Oncora Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Folixia (Multivitamin).
What is the active ingredient?: Ferrous bisglycinate, Potassium iodide, Pyridoxine hydrochloride, Beta carotene, Ascorbic acid, Cholecalciferol, Biotin, Folic acid, Cyanocobalamin, Calcium carbonate, Magnesium oxide, .alpha.-tocopherol acetate, Dl-.
Who is the labeler?: Oncora Pharma, LLC, NDC labeler code 85477. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Folixia?: 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.

Folixia (Multivitamin) NDC 85477-902