What is NDC 59088-008?

59088-008 is the product NDC for Finazol, Vitamin a acetate 1500 ug/1 + 23 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?

Finazol (Ferrous Fumarate, Folate).

What is the active ingredient?

Vitamin a acetate, Ascorbic acid, Cholecalciferol, .alpha.-tocopherol acetate, Dl-, Thiamine mononitrate, Riboflavin, Niacinamide, Pyridoxine hydrochloride, Levomefolate calcium, Methylcobalamin, Biotin, Pantothenic acid, Calcium carbonate, Ferrous fumarate, Potassium iodide, Magnesium oxide, Zinc citrate, Selenium, Cuprous oxide, Manganese sulfate, Chromium nicotinate, Molybdenum, Potassium chloride, Boron.

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 Finazol?

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.

Finazol NDC 59088-008 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-008Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0008Add 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
59088-008-54	5908800085459088000854	30 TABLET in 1 BOTTLE, PLASTIC (59088-008-54)Marketed from Oct 11, 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): Finazol
Generic name (nonproprietary): ferrous fumarate, folate
Active ingredients: Vitamin a acetate — 1500 ug/1Ascorbic acid — 200 mg/1Cholecalciferol — 10 ug/1.alpha.-tocopherol acetate, Dl- — 45 mg/1Thiamine mononitrate — 3.25 mg/1Riboflavin — 3.35 mg/1Niacinamide — 22.5 mg/1Pyridoxine hydrochloride — 6 mg/1Levomefolate calcium — 1000 ug/1Methylcobalamin — 26 ug/1Biotin — 100 ug/1Pantothenic acid — 15 mg/1Calcium carbonate — 100 mg/1Ferrous fumarate — 18 mg/1Potassium iodide — 25 ug/1Magnesium oxide — 50 mg/1Zinc citrate — 30 mg/1Selenium — 30 ug/1Cuprous oxide — 1 mg/1Manganese sulfate — .75 mg/1Chromium nicotinate — 37.5 ug/1Molybdenum — 25 ug/1Potassium chloride — 24.5 mg/1Boron — 25 ug/1
Dosage form: Tablet
Route: Oral
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Oct 11, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Analogs/Derivatives (Chemical/Ingredient)Ascorbic Acid (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Decreased Copper Ion Absorption (Physiologic effect)Folic Acid (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (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)Nicotinic Acids (Chemical structure)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Potassium Compounds (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)Vitamin A (Chemical structure)Vitamin B 6 (Chemical/Ingredient)Vitamin D (Chemical structure)
Identifiers: Product ID 59088-008_2657fc47-d75d-ff7d-e063-6394a90a68eeSPL ID 2657fc47-d75d-ff7d-e063-6394a90a68eeSPL set ID 24290823-022a-433b-e063-6394a90a8fd0UNII 3LE3D9D6OY, PQ6CK8PD0R, 1C6V77QF41, WR1WPI7EW8, 8K0I04919X, TLM2976OFR, 25X51I8RD4, 68Y4CF58BV, A9R10K3F2F, BR1SN1JS2W, 6SO6U10H04, 19F5HK2737, H0G9379FGK, R5L488RY0Q, 1C4QK22F9J, 3A3U0GI71G, K72I3DEX9B, H6241UJ22B, T8BEA5064F, W00LYS4T26, A150AY412V, 81AH48963U, 660YQ98I10, N9E3X5056Q
Pharmacologic class: Blood Coagulation Factor; Calculi Dissolution Agent; Copper Absorption Inhibitor; Folate Analog; Nicotinic Acid; Osmotic Laxative; Paramagnetic Contrast Agent; Phosphate Binder; Potassium Salt; 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

N459088000854 followed by a unit qualifier and the quantity

Package 59088-0008-54. 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 Nov 7, 2024.

Indications (excerpt from the label)

INDICATIONS: Finazol™ is indicated for iron deficiency anemia and folate deficiency as in extended convalescence, menorrhagia, pregnancy, puberty, excessive blood loss and advanced age. Also, for conditions in which iron deficiency and vitamin C deficiency occur together, along with a deficient intake or increased need for B-Complex vitamins in chronic and acute illness, as well as cases of metabolic stress, and in convalescence.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59088-008

What is NDC 59088-008?: 59088-008 is the product NDC for Finazol, Vitamin a acetate 1500 ug/1 + 23 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?: Finazol (Ferrous Fumarate, Folate).
What is the active ingredient?: Vitamin a acetate, Ascorbic acid, Cholecalciferol, .alpha.-tocopherol acetate, Dl-, Thiamine mononitrate, Riboflavin, Niacinamide, Pyridoxine hydrochloride, Levomefolate calcium, Methylcobalamin, Biotin, Pantothenic acid, Calcium carbonate, Ferrous fumarate, Potassium iodide, Magnesium oxide, Zinc citrate, Selenium, Cuprous oxide, Manganese sulfate, Chromium nicotinate, Molybdenum, Potassium chloride, Boron.
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 Finazol?: 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.

Finazol (Ferrous fumarate, folate) NDC 59088-008