NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2845Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2845Add 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
71335-2845-17133528450115 g in 1 BOTTLE, PLASTIC (71335-2845-1)Marketed from Oct 21, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Nystop
Generic name (nonproprietary)
nystatin
Active ingredients
Nystatin — 100000 [USP'U]/g
Dosage form
Powder
Route
Topical
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 064118
Marketing start
Listing expires
Other FDA classes
Polyenes (Chemical structure)
Identifiers
Product ID 71335-2845_0cf86c4a-028c-48d9-88cf-937059ecd907SPL ID 0cf86c4a-028c-48d9-88cf-937059ecd907SPL set ID 64041bdf-1207-47f6-93f3-bc4656a7d2aeRxCUI 261178, 646456UNII BDF1O1C72E
Pharmacologic class
Polyene Antifungal

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471335284501 followed by a unit qualifier and the quantity

Package 71335-2845-01. 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 Nystatin Topical Powder is indicated in the treatment of cutaneous or mucocutaneous mycotic infections caused by Candida albicans and other susceptible Candida species. This preparation is not indicated for systemic, oral, intravaginal or ophthalmic use.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2845

What is NDC 71335-2845?
71335-2845 is the product NDC for Nystop (nystatin), Nystatin 100000 [USP'U]/g powder, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Nystop (Nystatin).
What is the active ingredient?
Nystatin.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nystop?
6 other product NDCs are listed under this name. See all Nystop 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 Nystop NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
NystopnystatinNystatin 100000 [USP'U]/gPowderTopicalPadagis US LLC0574-200800574-2008-0200574-2008-1500574-2008-30
NystopnystatinNystatin 100000 [USP'U]/gPowderTopicalBryant Ranch Prepack63629-869663629-8696-01
NystopnystatinNystatin 100000 [USP'U]/gPowderTopicalBryant Ranch Prepack63629-869763629-8697-01
NystopnystatinNystatin 100000 [USP'U]/gPowderTopicalBryant Ranch Prepack63629-869863629-8698-01
NystopnystatinNystatin 100000 [USP'U]/gPowderTopicalBryant Ranch Prepack71335-286971335-2869-01
NystopnystatinNystatin 100000 [USP'U]/gPowderTopicalBryant Ranch Prepack72162-112472162-1124-0272162-1124-0372162-1124-06

Other NDCs under ANDA 064118

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

FDA NDC Directory listings under ANDA 064118
ProductStrengthForm · routeLabelerProduct NDC
NystatinNystatin 100000 [USP'U]/gPowderTopicalNorthstar Rx LLC72603-491
NystopnystatinNystatin 100000 [USP'U]/gPowderTopicalPadagis US LLC0574-2008
NystopnystatinNystatin 100000 [USP'U]/gPowderTopicalBryant Ranch Prepack63629-8696
NystopnystatinNystatin 100000 [USP'U]/gPowderTopicalBryant Ranch Prepack63629-8697
NystopnystatinNystatin 100000 [USP'U]/gPowderTopicalBryant Ranch Prepack63629-8698
NystopnystatinNystatin 100000 [USP'U]/gPowderTopicalBryant Ranch Prepack71335-2869
NystopnystatinNystatin 100000 [USP'U]/gPowderTopicalBryant Ranch Prepack72162-1124

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