What is NDC 59088-018?

59088-018 is the product NDC for Multivitamin, Vitamin a 750 ug/1 + 10 more ingredients tablet, chewable, 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?

Vitamin a, Ascorbic acid, Sodium ascorbate, Cholecalciferol, .alpha.-tocopherol acetate, Dl-, Pyridoxine hydrochloride, Thiamine mononitrate, Riboflavin, Niacin, Levomefolate calcium, Methylcobalamin.

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 Multivitamin?

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.

Multivitamin NDC 59088-018 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-018Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0018Add 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
59088-018-54	59088001854	30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (59088-018-54)Marketed from May 15, 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): Multivitamin
Generic name (nonproprietary): multivitamin
Active ingredients: Vitamin a — 750 ug/1Ascorbic acid — 24 mg/1Sodium ascorbate — 36 mg/1Cholecalciferol — 10 ug/1.alpha.-tocopherol acetate, Dl- — 10 mg/1Pyridoxine hydrochloride — 1.05 mg/1Thiamine mononitrate — 1.05 mg/1Riboflavin — 1.2 mg/1Niacin — 13.5 mg/1Levomefolate calcium — 1000 ug/1Methylcobalamin — 4.5 ug/1
Dosage form: Tablet, Chewable
Route: Oral
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: May 15, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Analogs/Derivatives (Chemical/Ingredient)Ascorbic Acid (Chemical structure)Ascorbic Acid (Chemical structure)Folic Acid (Chemical structure)Nicotinic Acids (Chemical structure)Vitamin A (Chemical structure)Vitamin B 6 (Chemical/Ingredient)Vitamin D (Chemical structure)
Identifiers: Product ID 59088-018_353453e2-1f60-24ea-e063-6394a90a251eSPL ID 353453e2-1f60-24ea-e063-6394a90a251eSPL set ID 353453e2-1f60-24ea-e063-6394a90a251eUNII 81G40H8B0T, PQ6CK8PD0R, S033EH8359, 1C6V77QF41, WR1WPI7EW8, 68Y4CF58BV, 8K0I04919X, TLM2976OFR, 2679MF687A, A9R10K3F2F, BR1SN1JS2WUPC 0359088018545
Pharmacologic class: Folate Analog; Nicotinic Acid; Vitamin A; 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

N459088001854 followed by a unit qualifier and the quantity

Package 59088-0018-54. 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 May 15, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Multivitamin Chewable Tablets is indicated to provide significant amounts of Vitamins A, C, D, E, thiamine, riboflavin, niacin, vitamin B6, vitamin B12, and folate to supplement the diet, and to help assure that nutritional deficiencies of these vitamins will not develop. Contraindications: This product is contraindicated in patients with known hypersensitivity to any of its ingredients.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59088-018

What is NDC 59088-018?: 59088-018 is the product NDC for Multivitamin, Vitamin a 750 ug/1 + 10 more ingredients tablet, chewable, 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?: Multivitamin.
What is the active ingredient?: Vitamin a, Ascorbic acid, Sodium ascorbate, Cholecalciferol, .alpha.-tocopherol acetate, Dl-, Pyridoxine hydrochloride, Thiamine mononitrate, Riboflavin, Niacin, Levomefolate calcium, Methylcobalamin.
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 Multivitamin?: 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.