What is NDC 59088-301?

59088-301 is the product NDC for Folixate, Levomefolate calcium 1000 ug/1; Vitamin d 125 ug/1 tablet, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Levomefolate calcium, Vitamin d.

PureTek Corporation, NDC labeler code 59088. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Folixate?

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.

Folixate NDC 59088-301 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-301Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0301Add 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
59088-301-54	5908803015459088030154	30 TABLET in 1 BOTTLE, PLASTIC (59088-301-54)Marketed from Dec 5, 2023

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): Folixate
Generic name (nonproprietary): folate, vitamin d3
Active ingredients: Levomefolate calcium — 1000 ug/1Vitamin d — 125 ug/1
Dosage form: Tablet
Route: Oral
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Dec 5, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Folic Acid (Chemical structure)Vitamin D (Chemical structure)
Identifiers: Product ID 59088-301_0bb91f61-b61a-c894-e063-6394a90ae51cSPL ID 0bb91f61-b61a-c894-e063-6394a90ae51cSPL set ID 0bb91f61-b61b-c894-e063-6394a90ae51cRxCUI 2671090, 2671097UNII A9R10K3F2F, 9VU1KI44GPUPC 0359088301548
Pharmacologic class: Folate Analog; 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

N459088030154 followed by a unit qualifier and the quantity

Package 59088-0301-54. 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 Dec 5, 2023.

Indications (excerpt from the label)

INDICATIONS AND USAGE Folixate ™ is indicated for dietary management of patients with unique nutritional needs requiring increased folate level and Vitamin D supplementation. Folixate™ can be taken by women of childbearing age, pregnant women, and lactating and nonlactating mothers.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59088-301

What is NDC 59088-301?: 59088-301 is the product NDC for Folixate, Levomefolate calcium 1000 ug/1; Vitamin d 125 ug/1 tablet, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Folixate (Folate, Vitamin D3).
What is the active ingredient?: Levomefolate calcium, Vitamin d.
Who is the labeler?: PureTek Corporation, NDC labeler code 59088. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Folixate?: 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.

Folixate (Folate, vitamin d3) NDC 59088-301