NDC codes

FDA NDC Directory
Product NDC (as listed)23155-865Labeler and product segments. Claims need a package NDC.
Product NDC at billing width23155-0865Add 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
23155-865-012315508650123155086501100 TABLET in 1 BOTTLE, PLASTIC (23155-865-01)Marketed from Jun 30, 2023

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)
Griseofulvin Microsize
Generic name (nonproprietary)
griseofulvin
Active ingredients
Griseofulvin — 500 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 060569
Marketing start
Listing expires
Other FDA classes
Decreased Mitosis (Physiologic effect)Microtubule Inhibition (Physiologic effect)
Identifiers
Product ID 23155-865_d6360b00-96f1-4508-82e8-8425f8393851SPL ID d6360b00-96f1-4508-82e8-8425f8393851SPL set ID 1c26d7a6-17d9-4a95-a4ee-cfc5fe6bb95dRxCUI 310600UNII 32HRV3E3D5
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

N423155086501 followed by a unit qualifier and the quantity

Package 23155-0865-01. 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)

INDICASTIONS AND USAGE Griseofulvin tablets, USP are indicated for the treatment of dermatophyte infections of the skin not adequately treated by topical therapy, hair and nails, namely: Tinea corporis Tinea pedis Tinea cruris Tinea barbae Tinea capitis Tinea unguium when caused by one or more of the following species of fungi: Epidermophyton floccosum Microsporum audouinii Microsporum canis Microsporum gypseum Trichophyton crateriform Trichophyton gallinae Trichophyton interdigitalis Trichophyton megnini Trichophyton mentagrophytes Trichophyton rubrum Trichophyton schoenleini Trichophyton sulphureum Trichophyton tonsurans Trichophyton verrucosum Note: Prior to therapy, a dermatophyte should…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 23155-865

What is NDC 23155-865?
23155-865 is the product NDC for Griseofulvin Microsize (griseofulvin), Griseofulvin 500 mg/1 tablet, listed with the FDA by Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Griseofulvin Microsize (Griseofulvin).
What is the active ingredient?
Griseofulvin.
Who is the labeler?
Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc, NDC labeler code 23155. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Griseofulvin Microsize?
1 other product NDC are listed under this name. See all Griseofulvin Microsize 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 Griseofulvin Microsize NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Griseofulvin MICROSIZEgriseofulvinGriseofulvin 500 mg/1TabletOralChartwell RX, LLC.62135-49662135-0496-0162135-0496-30

Other NDCs under ANDA 060569

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

FDA NDC Directory listings under ANDA 060569
ProductStrengthForm · routeLabelerProduct NDC
Griseofulvin MICROSIZEgriseofulvinGriseofulvin 500 mg/1TabletOralChartwell RX, LLC.62135-496

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