What is NDC 51672-5292?

51672-5292 is the product NDC for psorcon (diflorasone diacetate), Diflorasone diacetate 5 mg/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 psorcon?

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.

psorcon NDC 51672-5292 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-5292Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-5292Add 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
51672-5292-3	5167252920351672529203	1 TUBE in 1 CARTON (51672-5292-3) / 60 g in 1 TUBEMarketed from Aug 1, 2014
51672-5292-5	5167252920551672529205	1 TUBE in 1 CARTON (51672-5292-5) / 5 g in 1 TUBEMarketed from Aug 1, 2014

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): psorcon
Generic name (nonproprietary): diflorasone diacetate
Active ingredients: Diflorasone diacetate — 5 mg/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 075508
Marketing start: Aug 1, 2014
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 51672-5292_38f8aa09-3cda-ae9a-e063-6294a90aa2f6SPL ID 38f8aa09-3cda-ae9a-e063-6294a90aa2f6SPL set ID de40cc65-f955-423f-9cbd-bc2245c4f982UNII 7W2J09SCWX
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

N451672529203 followed by a unit qualifier and the quantity

Package 51672-5292-03. 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 2, 2025.

Indications (excerpt from the label)

INDICATION AND USAGE PSORCON ® (diflorasone diacetate cream USP), 0.05% is a high potency corticosteroid 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 51672-5292

What is NDC 51672-5292?: 51672-5292 is the product NDC for psorcon (diflorasone diacetate), Diflorasone diacetate 5 mg/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?: psorcon (Diflorasone Diacetate).
What is the active ingredient?: Diflorasone diacetate.
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 psorcon?: 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.

Other NDCs under ANDA 075508

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

FDA NDC Directory listings under ANDA 075508
Product	Strength	Form · route	Labeler	Product NDC
Diflorasone Diacetate	Diflorasone diacetate .5 mg/g	CreamTopical	Sun Pharmaceutical Industries, Inc.	51672-1296

psorcon (Diflorasone diacetate) NDC 51672-5292