Ketoconazole NDC 68071-5294

NDC codes

FDA NDC Directory

Product NDC (as listed)68071-5294Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68071-5294Add 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
68071-5294-4	68071529404	120 mL in 1 BOTTLE (68071-5294-4)Marketed from Jun 2, 2026

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): Ketoconazole
Generic name (nonproprietary): ketoconazole
Active ingredients: Ketoconazole — 20 mg/mL
Dosage form: Shampoo, Suspension
Route: Topical
Labeler: NuCare Pharmaceuticals, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076419
Marketing start: Dec 1, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Azoles (Chemical structure)Cytochrome P450 3A4 Inhibitors (Mechanism)Cytochrome P450 3A5 Inhibitors (Mechanism)P-Glycoprotein Inhibitors (Mechanism)
Identifiers: Product ID 68071-5294_53492ad1-bacb-a7f6-e063-6294a90a2990SPL ID 53492ad1-bacb-a7f6-e063-6294a90a2990SPL set ID 53492ad1-baca-a7f6-e063-6294a90a2990RxCUI 106336UNII R9400W927IUPC 0368071529449
Pharmacologic class: Azole 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

N468071529404 followed by a unit qualifier and the quantity

Package 68071-5294-04. 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 Jun 2, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Ketoconazole Shampoo, 2% is indicated for the treatment of tinea (pityriasis) versicolor caused by or presumed to be caused by Pityrosporum orbiculare (also known as Malassezia furfur or M. orbiculare ) . Note: Tinea (pityriasis) versicolor may give rise to hyperpigmented or hypopigmented patches on the trunk which may extend to the neck, arms and upper thighs. Treatment of the infection may not immediately result in normalization of pigment to the affected sites. Normalization of pigment following successful therapy is variable and may take months, depending on individual skin type and incidental sun exposure. Although tinea versicolor is not contagious, it may recur b…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076419

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

FDA NDC Directory listings under ANDA 076419
Product	Strength	Form · route	Labeler	Product NDC
Ketoconazole	Ketoconazole 20 mg/mL	Shampoo, SuspensionTopical	Bryant Ranch Prepack	72162-1409
Ketoconazole	Ketoconazole 20 mg/mL	Shampoo, SuspensionTopical	NuCare Pharmaceuticals,Inc.	68071-3930
Ketoconazole	Ketoconazole 20 mg/mL	Shampoo, SuspensionTopical	Bryant Ranch Prepack	63629-8675
Ketoconazole	Ketoconazole 20 mg/mL	Shampoo, SuspensionTopical	Padagis Israel Pharmaceuticals Ltd	45802-465
Ketoconazole	Ketoconazole 20 mg/mL	Shampoo, SuspensionTopical	Bryant Ranch Prepack	71335-2839
Ketoconazole	Ketoconazole 20 mg/mL	Shampoo, SuspensionTopical	Northstar Rx LLC	72603-878