Econazole Nitrate NDC 68788-8174

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-8174Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-8174Add 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
68788-8174-1	68788817401	1 TUBE in 1 CARTON (68788-8174-1) / 15 g in 1 TUBEMarketed from Apr 27, 2022

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): Econazole Nitrate
Generic name (nonproprietary): econazole nitrate
Active ingredients: Econazole nitrate — 10 mg/g
Dosage form: Cream
Route: Topical
Labeler: Preferred Pharmaceuticals Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076005
Marketing start: Apr 27, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Azoles (Chemical structure)
Identifiers: Product ID 68788-8174_406c3588-6206-4be4-a148-47e489feed8fSPL ID 406c3588-6206-4be4-a148-47e489feed8fSPL set ID 6989d30f-9bb7-4e6e-92de-05e9f9a4f523RxCUI 857366UNII H438WYN10E
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

N468788817401 followed by a unit qualifier and the quantity

Package 68788-8174-01. 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 Apr 10, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Econazole nitrate cream is indicated for topical application in the treatment of tinea pedis, tinea cruris, and tinea corporis caused by Trichophyton rubrum, Trichophyton mentagrophytes, Trichophyton tonsurans, Microsporum canis, Microsporum audouini, Microsporum gypseum, and Epidermophyton floccosum, in the treatment of cutaneous candidiasis, and in the treatment of tinea versicolor.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076005

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

FDA NDC Directory listings under ANDA 076005
Product	Strength	Form · route	Labeler	Product NDC
Econazole Nitrate	Econazole nitrate 10 mg/g	CreamTopical	Sun Pharmaceutical Industries, Inc.	51672-1303