NDC codes

FDA NDC Directory
Product NDC (as listed)42794-014Labeler and product segments. Claims need a package NDC.
Product NDC at billing width42794-0014Add 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 NDC11-digit (billing)PackageCopy
42794-014-08427940014084279400140830 TABLET in 1 BOTTLE (42794-014-08)Marketed from May 11, 2016

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)
Ultramicrosize Griseofulvin
Generic name (nonproprietary)
ultramicrosize griseofulvin
Active ingredients
Griseofulvin — 250 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Sigmapharm Laboratories, LLCNDC labeler code 42794
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202545
Marketing start
Listing expires
Other FDA classes
Decreased Mitosis (Physiologic effect)Microtubule Inhibition (Physiologic effect)
Identifiers
Product ID 42794-014_d58d8124-4925-b8a1-e053-2995a90ac4c5SPL ID d58d8124-4925-b8a1-e053-2995a90ac4c5SPL set ID 37b4d132-84f1-4394-b468-7e74eeec61ebRxCUI 239239, 242831UNII 32HRV3E3D5UPC 0342794013089, 0342794014086
Pharmacologic class
Tubulin Inhibiting 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

N442794001408 followed by a unit qualifier and the quantity

Package 42794-0014-08. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Ultramicrosize Griseofulvin Tablets, USP are indicated for the treatment of the following ringworm infections; tinea corporis (ringworm of the body), tinea pedis (athlete's foot), tinea cruris (ringworm of the groin and thigh), tinea barbae (barber's itch), tinea capitis (ringworm of the scalp), and tinea unguium (onychomycosis, ringworm of the nails), when caused by one or more of the following genera of fungi: Trichophyton rubrum, Trichophyton tonsurans, Trichophyton mentagrophytes, Trichophyton interdigitalis, Trichophyton verrucosum, Trichophyton megnini, Trichophyton gallinae, Trichophyton crateriform, Trichophyton sulphureum, Trichophyton schoenleini, Microsporum …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 42794-014

What is NDC 42794-014?
42794-014 is the product NDC for Ultramicrosize Griseofulvin, Griseofulvin 250 mg/1 tablet, listed with the FDA by Sigmapharm Laboratories, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ultramicrosize Griseofulvin.
What is the active ingredient?
Griseofulvin.
Who is the labeler?
Sigmapharm Laboratories, LLC, NDC labeler code 42794. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ultramicrosize Griseofulvin?
11 other product NDCs are listed under this name. See all Ultramicrosize Griseofulvin NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Ultramicrosize Griseofulvin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Ultramicrosize GriseofulvingriseofulvinGriseofulvin 125 mg/1TabletOralHeritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc23155-86323155-0863-01
Ultramicrosize GriseofulvingriseofulvinGriseofulvin 250 mg/1TabletOralHeritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc23155-86423155-0864-01
Ultramicrosize GriseofulvinGriseofulvin 125 mg/1Tablet, CoatedOralSandoz Inc0781-582700781-5827-0100781-5827-05
Ultramicrosize GriseofulvinGriseofulvin 250 mg/1Tablet, CoatedOralSandoz Inc0781-582800781-5828-0100781-5828-05
Ultramicrosize Griseofulvinultramicrosize griseofulvin tabletsGriseofulvin 125 mg/1Tablet, CoatedOralAmneal Pharmaceuticals of New York LLC0115-172400115-1724-0100115-1724-02
Ultramicrosize Griseofulvinultramicrosize griseofulvin tabletsGriseofulvin 250 mg/1Tablet, CoatedOralAmneal Pharmaceuticals of New York LLC0115-172500115-1725-0100115-1725-03
Ultramicrosize GriseofulvinGriseofulvin 125 mg/1TabletOralSigmapharm Laboratories, LLC42794-01342794-0013-08
Ultramicrosize GriseofulvingriseofulvinGriseofulvin 125 mg/1TabletOralChartwell RX, LLC.62135-49462135-0494-0162135-0494-30
Ultramicrosize GriseofulvingriseofulvinGriseofulvin 250 mg/1TabletOralChartwell RX, LLC.62135-49562135-0495-0162135-0495-30
Ultramicrosize GriseofulvinGriseofulvin 165 mg/1TabletOralChartwell RX, LLC62135-50162135-0501-30

All 12 Ultramicrosize Griseofulvin NDCs

Other NDCs under ANDA 202545

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 202545
ProductStrengthForm · routeLabelerProduct NDC
Ultramicrosize GriseofulvinGriseofulvin 125 mg/1TabletOralSigmapharm Laboratories, LLC42794-013

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