What is NDC 42192-374?

42192-374 is the product NDC for Nicotinamide, Niacinamide 750 mg/1 + 5 more ingredients tablet, listed with the FDA by Acella Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Niacinamide, Zinc glycinate, Levomefolate calcium, Cupric oxide, Selenium, Chromium.

Acella Pharmaceuticals, LLC, NDC labeler code 42192. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Nicotinamide?

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.

Nicotinamide NDC 42192-374 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)42192-374Labeler and product segments. Claims need a package NDC.

Product NDC at billing width42192-0374Add 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
42192-374-60	4219203746042192037460	60 TABLET in 1 BOTTLE (42192-374-60)Marketed from May 25, 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): Nicotinamide
Generic name (nonproprietary): nicotinamide
Active ingredients: Niacinamide — 750 mg/1Zinc glycinate — 27 mg/1Levomefolate calcium — 500 ug/1Cupric oxide — 2 mg/1Selenium — 50 ug/1Chromium — 100 ug/1
Dosage form: Tablet
Route: Oral
Labeler: Acella Pharmaceuticals, LLCNDC labeler code 42192
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: May 25, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Decreased Copper Ion Absorption (Physiologic effect)Folic Acid (Chemical structure)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 42192-374_55f85d14-1d83-20e5-e063-6294a90aa945SPL ID 55f85d14-1d83-20e5-e063-6294a90aa945
Pharmacologic class: Copper Absorption Inhibitor; Folate Analog; Standardized Chemical Allergen

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

N442192037460 followed by a unit qualifier and the quantity

Package 42192-0374-60. 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 42192-374

What is NDC 42192-374?: 42192-374 is the product NDC for Nicotinamide, Niacinamide 750 mg/1 + 5 more ingredients tablet, listed with the FDA by Acella Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Nicotinamide.
What is the active ingredient?: Niacinamide, Zinc glycinate, Levomefolate calcium, Cupric oxide, Selenium, Chromium.
Who is the labeler?: Acella Pharmaceuticals, LLC, NDC labeler code 42192. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nicotinamide?: 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.