What is NDC 51672-4166?

51672-4166 is the product NDC for Clocortolone Pivalate, Clocortolone pivalate .001 g/g cream, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Clocortolone Pivalate?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Clocortolone Pivalate NDC 51672-4166 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-4166Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-4166Add 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
51672-4166-6	51672416606	1 TUBE in 1 CARTON (51672-4166-6) / 45 g in 1 TUBEMarketed from Apr 21, 2020
51672-4166-8	51672416608	1 TUBE in 1 CARTON (51672-4166-8) / 90 g in 1 TUBEMarketed from Apr 21, 2020

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): Clocortolone Pivalate
Generic name (nonproprietary): clocortolone pivalate
Active ingredients: Clocortolone pivalate — .001 g/g
Dosage form: Cream
Route: Topical
Labeler: Sun Pharmaceutical Industries, Inc.NDC labeler code 51672
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 206370
Marketing start: Apr 21, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 51672-4166_56996baf-3d54-9d1e-e063-6394a90ab576SPL ID 56996baf-3d54-9d1e-e063-6394a90ab576SPL set ID 88d9a7cf-31b5-4b85-9827-0ecce328e6a0RxCUI 197520UNII QBL8IZH14X
Pharmacologic class: Corticosteroid

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

N451672416606 followed by a unit qualifier and the quantity

Package 51672-4166-06. 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 Jul 14, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Topical corticosteroids are indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51672-4166

What is NDC 51672-4166?: 51672-4166 is the product NDC for Clocortolone Pivalate, Clocortolone pivalate .001 g/g cream, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Clocortolone Pivalate.
What is the active ingredient?: Clocortolone pivalate.
Who is the labeler?: Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Clocortolone Pivalate?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.