What is NDC 59088-795?

59088-795 is the product NDC for Folcyteine (multivitamin), Calcium citrate 47 mg/1 + 4 more ingredients 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?

Calcium citrate, Cholecalciferol, Folic acid, Acetylcysteine, Magnesium citrate.

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 Folcyteine?

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.

Folcyteine NDC 59088-795 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-795Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0795Add 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
59088-795-54	5908807955459088079554	30 TABLET in 1 BOTTLE, PLASTIC (59088-795-54)Marketed from Sep 14, 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): Folcyteine
Generic name (nonproprietary): multivitamin
Active ingredients: Calcium citrate — 47 mg/1Cholecalciferol — 800 [iU]/1Folic acid — 1000 ug/1Acetylcysteine — 200 mg/1Magnesium citrate — 16 mg/1
Dosage form: Tablet
Route: Oral
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Sep 14, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Coagulation Factor Activity (Physiologic effect)Increased Glutathione Concentration (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)Reduction Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)Vitamin D (Chemical structure)
Identifiers: Product ID 59088-795_5592f382-e77e-a812-e063-6294a90a905cSPL ID 5592f382-e77e-a812-e063-6294a90a905cSPL set ID 04cf0026-e29b-ffd5-e063-6294a90aca1fUNII MLM29U2X85, 1C6V77QF41, 935E97BOY8, WYQ7N0BPYC, RHO26O1T9VUPC 0359088795545
Pharmacologic class: Antidote; Antidote for Acetaminophen Overdose; Blood Coagulation Factor; Calculi Dissolution Agent; Mucolytic; Osmotic Laxative; Phosphate Binder; 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

N459088079554 followed by a unit qualifier and the quantity

Package 59088-0795-54. 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 Jul 8, 2026.

Indications (excerpt from the label)

Indications and Usage : Folcyteine™ is indicated as a vitamin, mineral supplementation for adult men and women. Folic acid is used to treat megaloblastic anemia caused by folic acid deficiency, including cases associated with tropical or nontropical sprue, as well as anemia due to nutritional deficiency or pregnancy.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59088-795

What is NDC 59088-795?: 59088-795 is the product NDC for Folcyteine (multivitamin), Calcium citrate 47 mg/1 + 4 more ingredients 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?: Folcyteine (Multivitamin).
What is the active ingredient?: Calcium citrate, Cholecalciferol, Folic acid, Acetylcysteine, Magnesium citrate.
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 Folcyteine?: 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.

Folcyteine (Multivitamin) NDC 59088-795