Clotrimazole NDC 51672-1275

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-1275Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-1275Add 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
51672-1275-1	51672127501	1 TUBE in 1 CARTON (51672-1275-1) / 15 g in 1 TUBEMarketed from Aug 31, 1993
51672-1275-2	51672127502	1 TUBE in 1 CARTON (51672-1275-2) / 30 g in 1 TUBEMarketed from Aug 31, 1993
51672-1275-6	51672127506	1 TUBE in 1 CARTON (51672-1275-6) / 45 g in 1 TUBEMarketed from Aug 31, 1993
51672-1275-7	51672127507	2 TUBE in 1 CARTON (51672-1275-7) / 45 g in 1 TUBEMarketed from Aug 31, 1993

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): Clotrimazole
Generic name (nonproprietary): clotrimazole
Active ingredients: Clotrimazole — 10 mg/g
Dosage form: Cream
Route: Topical
Labeler: Sun Pharmaceutical Industries, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 072640
Marketing start: Aug 31, 1993
Listing expires: Dec 31, 2026
Other FDA classes: Azoles (Chemical structure)
Identifiers: Product ID 51672-1275_3e748b32-1a66-10b0-e063-6394a90a7321SPL ID 3e748b32-1a66-10b0-e063-6394a90a7321SPL set ID 77883cfd-f13c-40cb-88b2-8f777e1cdce9RxCUI 309367UNII G07GZ97H65UPC 0351672127565
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

N451672127501 followed by a unit qualifier and the quantity

Package 51672-1275-01. 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 Sep 10, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Clotrimazole cream USP is indicated for the topical treatment of candidiasis due to Candida albicans and tinea versicolor due to Malassezia furfur . Clotrimazole is also available as a nonprescription item which is indicated for the topical treatment of the following dermal infections: tinea pedis, tinea cruris, and tinea corporis due to Trichophyton rubrum, Trichophyton mentagrophytes, Epidermophyton floccosum, and Microsporum canis .

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 072640

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

FDA NDC Directory listings under ANDA 072640
Product	Strength	Form · route	Labeler	Product NDC
Clotrimazole	Clotrimazole 10 mg/g	CreamTopical	Proficient Rx LP	71205-432