What is NDC 51672-4193?

51672-4193 is the product NDC for Clobetasol Propionate, Clobetasol propionate .5 mg/g aerosol, foam, 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 Clobetasol Propionate?

102 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Clobetasol Propionate NDC 51672-4193 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-4193Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-4193Add 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
51672-4193-3	51672419303	1 CAN in 1 CARTON (51672-4193-3) / 50 g in 1 CANMarketed from Oct 4, 2018
51672-4193-7	51672419307	1 CAN in 1 CARTON (51672-4193-7) / 100 g in 1 CANMarketed from Oct 4, 2018

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): Clobetasol Propionate
Generic name (nonproprietary): clobetasol propionate
Active ingredients: Clobetasol propionate — .5 mg/g
Dosage form: Aerosol, Foam
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 208779
Marketing start: Oct 4, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 51672-4193_56995638-47fc-8fb2-e063-6394a90ad083SPL ID 56995638-47fc-8fb2-e063-6394a90ad083SPL set ID d8f560c8-e223-46f0-8afb-b418f2b6399cRxCUI 861353UNII 779619577M
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

N451672419303 followed by a unit qualifier and the quantity

Package 51672-4193-03. 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 14, 2026.

Indications (excerpt from the label)

Clobetasol propionate foam is a corticosteroid indicated for treatment of moderate to severe plaque psoriasis of the scalp and mild to moderate plaque psoriasis of non-scalp regions of the body excluding the face and intertriginous areas in patients 12 years and older. Clobetasol propionate foam is a corticosteroid indicated for treatment of moderate to severe plaque psoriasis of the scalp and mild to moderate plaque psoriasis of non-scalp regions of the body excluding the face and intertriginous areas in patients 12 years and older. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51672-4193

What is NDC 51672-4193?: 51672-4193 is the product NDC for Clobetasol Propionate, Clobetasol propionate .5 mg/g aerosol, foam, 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?: Clobetasol Propionate.
What is the active ingredient?: Clobetasol propionate.
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 Clobetasol Propionate?: 102 other product NDCs are listed under this name. See all Clobetasol Propionate NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Clobetasol Propionate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Clobetasol Propionate	Clobetasol propionate .5 mg/g	OintmentTopical	A-S Medication Solutions	50090-8001	50090-8001-00
Clobetasol Propionate	Clobetasol propionate .5 mg/g	OintmentTopical	NorthStar RxLLC	72603-855	72603-0855-0172603-0855-0272603-0855-03+1 more
Clobetasol Propionate	Clobetasol propionate .5 mg/g	Aerosol, FoamTopical	Alembic Pharmaceuticals Limited	46708-707	46708-0707-3146708-0707-50
Clobetasol Propionate	Clobetasol propionate .5 mg/g	CreamTopical	Alembic Pharmaceuticals Limited	46708-547	46708-0547-1546708-0547-3046708-0547-45+1 more
Clobetasol Propionate	Clobetasol propionate .05 g/100mL	ShampooTopical	Alembic Pharmaceuticals Limited	46708-548	46708-0548-04
Clobetasol Propionate	Clobetasol propionate .5 mg/mL	SolutionTopical	Alembic Pharmaceuticals Limited	46708-486	46708-0486-2546708-0486-50
Clobetasol Propionate	Clobetasol propionate .05 g/mL	SprayTopical	Alembic Pharmaceuticals Limited	46708-425	46708-0425-1246708-0425-59
Clobetasol Propionate	Clobetasol propionate .5 mg/g	OintmentTopical	Alembic Pharmaceuticals Limited	46708-465	46708-0465-1546708-0465-3046708-0465-45+1 more
Clobetasol Propionate	Clobetasol propionate .25 mg/g	CreamTopical	INA Pharmaceutics Inc	74157-710	74157-0710-10
Clobetasol Propionate	Clobetasol propionate .5 mg/g	CreamTopical	Torrent Pharmaceuticals Limited	13668-569	13668-0569-0113668-0569-0213668-0569-04+1 more

All 103 Clobetasol Propionate NDCs