NDC codes

FDA NDC Directory
Product NDC (as listed)0781-5827Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00781-5827Add 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
0781-5827-010078158270100781582701100 TABLET, COATED in 1 BOTTLE (0781-5827-01)Marketed from Apr 1, 2020
0781-5827-050078158270500781582705500 TABLET, COATED in 1 BOTTLE (0781-5827-05)Marketed from Apr 1, 2020

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 125 mg/1
Dosage form
Tablet, Coated
Route
Oral
Labeler
Sandoz IncNDC labeler code 0781
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202805
Marketing start
Listing expires
Other FDA classes
Decreased Mitosis (Physiologic effect)Microtubule Inhibition (Physiologic effect)
Identifiers
Product ID 0781-5827_6d66c19d-0069-4a47-a45c-567aa0398135SPL ID 6d66c19d-0069-4a47-a45c-567aa0398135SPL set ID f4fa0eb9-bd6a-4ea2-b565-e0db88aa1ebdRxCUI 239239, 242831UNII 32HRV3E3D5UPC 0307815828011, 0307815827014
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

N400781582701 followed by a unit qualifier and the quantity

Package 00781-5827-01. 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)

INDICATIONS AND USAGE Ultramicrosize griseofulvin tablets 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 audou…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0781-5827

What is NDC 0781-5827?
0781-5827 is the product NDC for Ultramicrosize Griseofulvin, Griseofulvin 125 mg/1 tablet, coated, listed with the FDA by Sandoz Inc. It has 2 package NDCs, 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?
Sandoz Inc, NDC labeler code 0781. 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 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 GriseofulvinGriseofulvin 250 mg/1TabletOralSigmapharm Laboratories, LLC42794-01442794-0014-08
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 202805

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

FDA NDC Directory listings under ANDA 202805
ProductStrengthForm · routeLabelerProduct NDC
Ultramicrosize GriseofulvinGriseofulvin 250 mg/1Tablet, CoatedOralSandoz Inc0781-5828

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