What is NDC 59088-193?

59088-193 is the product NDC for Vitramyn (folic acid), Riboflavin 3.4 mg/1 + 16 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?

Riboflavin, Niacinamide, Ascorbic acid, Folic acid, Cyanocobalamin, Calcium carbonate, Vitamin a acetate, Thiamine mononitrate, Zinc oxide, Manganese sulfate, .alpha.-tocopherol acetate, Dl-, Magnesium oxide, Chromium nicotinate, Pyridoxine hydrochloride, Molybdenum, Selenium, Cholecalciferol.

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 Vitramyn?

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.

Vitramyn NDC 59088-193 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-193Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0193Add 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
59088-193-54	5908801935459088019354	30 TABLET in 1 BOTTLE, PLASTIC (59088-193-54)Marketed from Aug 20, 2021

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): Vitramyn
Generic name (nonproprietary): folic acid
Active ingredients: Riboflavin — 3.4 mg/1Niacinamide — 20 mg/1Ascorbic acid — 120 mg/1Folic acid — 1000 ug/1Cyanocobalamin — 8 ug/1Calcium carbonate — 200 mg/1Vitamin a acetate — 1500 ug/1Thiamine mononitrate — 3 mg/1Zinc oxide — 25 mg/1Manganese sulfate — 2.3 mg/1.alpha.-tocopherol acetate, Dl- — 30 mg/1Magnesium oxide — 200 mg/1Chromium nicotinate — 35 ug/1Pyridoxine hydrochloride — 20 mg/1Molybdenum — 45 ug/1Selenium — 55 ug/1Cholecalciferol — 20 ug/1
Dosage form: Tablet
Route: Oral
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Aug 20, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Analogs/Derivatives (Chemical/Ingredient)Ascorbic Acid (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Decreased Copper Ion Absorption (Physiologic effect)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)Magnetic Resonance Contrast Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)Vitamin A (Chemical structure)Vitamin B 12 (Chemical structure)Vitamin B 6 (Chemical/Ingredient)Vitamin D (Chemical structure)
Identifiers: Product ID 59088-193_548ee394-41b9-d346-e063-6394a90a0773SPL ID 548ee394-41b9-d346-e063-6394a90a0773SPL set ID c8af7616-5178-6df0-e053-2a95a90a334dUNII TLM2976OFR, 25X51I8RD4, PQ6CK8PD0R, 935E97BOY8, P6YC3EG204, H0G9379FGK, 3LE3D9D6OY, 8K0I04919X, SOI2LOH54Z, W00LYS4T26, WR1WPI7EW8, 3A3U0GI71G, A150AY412V, 68Y4CF58BV, 81AH48963U, H6241UJ22B, 1C6V77QF41UPC 0359088193549
Pharmacologic class: Blood Coagulation Factor; Calculi Dissolution Agent; Copper Absorption Inhibitor; Osmotic Laxative; Paramagnetic Contrast Agent; Phosphate Binder; Vitamin A; 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

N459088019354 followed by a unit qualifier and the quantity

Package 59088-0193-54. 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 Jun 18, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE: Vitramyn™ tablets are formulated to provide daily vitamin supplementation for adult men and women, helping support overall nutritional wellness. With folate, Vitramyn™ may be especially beneficial for women during the pre-pregnancy, pregnancy, and post-pregnancy periods by supporting healthy folate levels and helping address anemia related to folate deficiency.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59088-193

What is NDC 59088-193?: 59088-193 is the product NDC for Vitramyn (folic acid), Riboflavin 3.4 mg/1 + 16 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?: Vitramyn (Folic Acid).
What is the active ingredient?: Riboflavin, Niacinamide, Ascorbic acid, Folic acid, Cyanocobalamin, Calcium carbonate, Vitamin a acetate, Thiamine mononitrate, Zinc oxide, Manganese sulfate, .alpha.-tocopherol acetate, Dl-, Magnesium oxide, Chromium nicotinate, Pyridoxine hydrochloride, Molybdenum, Selenium, Cholecalciferol.
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 Vitramyn?: 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.

Vitramyn (Folic acid) NDC 59088-193