What is NDC 59088-162?

59088-162 is the product NDC for Diatrol, Biotin 30 ug/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?

Diatrol (Vitamins and mineral).

What is the active ingredient?

Biotin, Vanadyl sulfate, Chromium nicotinate, Gymnema sylvestre leaf, Arginine hydrochloride, .alpha.-tocopherol acetate, Dl-, Phytonadione, Vitamin a, Ascorbic acid, Cholecalciferol, Pyridoxine hydrochloride, Thiamine mononitrate, Riboflavin, Niacinamide, Levomefolate calcium, Methylcobalamin, Pantothenic acid.

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 Diatrol?

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.

Diatrol NDC 59088-162 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-162Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0162Add 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
59088-162-54	5908801625459088016254	30 TABLET in 1 BOTTLE, PLASTIC (59088-162-54)Marketed from Jan 26, 2024

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): Diatrol
Generic name (nonproprietary): vitamins and mineral
Active ingredients: Biotin — 30 ug/1Vanadyl sulfate — 15 mg/1Chromium nicotinate — 200 ug/1Gymnema sylvestre leaf — 100 mg/1Arginine hydrochloride — 60 ug/1.alpha.-tocopherol acetate, Dl- — 13.5 mg/1Phytonadione — 90 ug/1Vitamin a — 900 ug/1Ascorbic acid — 50 mg/1Cholecalciferol — 18.75 ug/1Pyridoxine hydrochloride — 8 mg/1Thiamine mononitrate — 4 mg/1Riboflavin — 4 mg/1Niacinamide — 24 mg/1Levomefolate calcium — 1000 ug/1Methylcobalamin — 8 ug/1Pantothenic acid — 8 mg/1
Dosage form: Tablet
Route: Oral
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Jan 26, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Analogs/Derivatives (Chemical/Ingredient)Ascorbic Acid (Chemical structure)Folic Acid (Chemical structure)Increased Prothrombin Activity (Physiologic effect)Reversed Anticoagulation Activity (Physiologic effect)Vitamin A (Chemical structure)Vitamin B 6 (Chemical/Ingredient)Vitamin D (Chemical structure)Vitamin K (Chemical structure)
Identifiers: Product ID 59088-162_5a0fe8c6-c758-749c-e063-6294a90a8fd5SPL ID 5a0fe8c6-c758-749c-e063-6294a90a8fd5
Pharmacologic class: Folate Analog; Vitamin A; Vitamin B6 Analog; Vitamin C; Vitamin D; Vitamin K; Warfarin Reversal Agent

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

N459088016254 followed by a unit qualifier and the quantity

Package 59088-0162-54. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 59088-162

What is NDC 59088-162?: 59088-162 is the product NDC for Diatrol, Biotin 30 ug/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?: Diatrol (Vitamins and mineral).
What is the active ingredient?: Biotin, Vanadyl sulfate, Chromium nicotinate, Gymnema sylvestre leaf, Arginine hydrochloride, .alpha.-tocopherol acetate, Dl-, Phytonadione, Vitamin a, Ascorbic acid, Cholecalciferol, Pyridoxine hydrochloride, Thiamine mononitrate, Riboflavin, Niacinamide, Levomefolate calcium, Methylcobalamin, Pantothenic acid.
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 Diatrol?: 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.

Diatrol (Vitamins and mineral) NDC 59088-162