NDC codes

FDA NDC Directory
Product NDC (as listed)72603-855Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72603-0855Add 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 NDC11-digit (billing)PackageCopy
72603-855-0172603085501726030855011 TUBE in 1 CARTON (72603-855-01) / 15 g in 1 TUBEMarketed from Feb 1, 2026
72603-855-0272603085502726030855021 TUBE in 1 CARTON (72603-855-02) / 30 g in 1 TUBEMarketed from Feb 1, 2026
72603-855-0372603085503726030855031 TUBE in 1 CARTON (72603-855-03) / 45 g in 1 TUBEMarketed from Feb 1, 2026
72603-855-0472603085504726030855041 TUBE in 1 CARTON (72603-855-04) / 60 g in 1 TUBEMarketed from Feb 1, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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
Ointment
Route
Topical
Labeler
NorthStar RxLLCNDC labeler code 72603
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215990
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 72603-855_3d14fff7-f1af-4d15-96b4-88cfccad271fSPL ID 3d14fff7-f1af-4d15-96b4-88cfccad271fSPL set ID 3d14fff7-f1af-4d15-96b4-88cfccad271fRxCUI 861448UNII 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

N472603085501 followed by a unit qualifier and the quantity

Package 72603-0855-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Clobetasol propionate ointment is super-high potency corticosteroid formulations indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid- responsive dermatoses. Treatment beyond 2 consecutive weeks is not recommended, and the total dosage should not exceed 50 g/week because of the potential for the drug to suppress the hypothalamic-pituitary-adrenal (HPA) axis. Use in pediatric patients under 12 years of age is not recommended. As with other highly active corticosteroids, therapy should be discontinued when control has been achieved. If no improvement is seen within 2 weeks, reassessment of the diagnosis may be necessary.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72603-855

What is NDC 72603-855?
72603-855 is the product NDC for Clobetasol Propionate, Clobetasol propionate .5 mg/g ointment, listed with the FDA by NorthStar RxLLC. It has 4 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?
NorthStar RxLLC, NDC labeler code 72603. 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?
96 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Clobetasol PropionateClobetasol propionate .5 mg/gOintmentTopicalA-S Medication Solutions50090-800150090-8001-00
Clobetasol PropionateClobetasol propionate .5 mg/gAerosol, FoamTopicalAlembic Pharmaceuticals Limited46708-70746708-0707-3146708-0707-50
Clobetasol PropionateClobetasol propionate .5 mg/gCreamTopicalAlembic Pharmaceuticals Limited46708-54746708-0547-1546708-0547-3046708-0547-45+1 more
Clobetasol PropionateClobetasol propionate .05 g/100mLShampooTopicalAlembic Pharmaceuticals Limited46708-54846708-0548-04
Clobetasol PropionateClobetasol propionate .5 mg/mLSolutionTopicalAlembic Pharmaceuticals Limited46708-48646708-0486-2546708-0486-50
Clobetasol PropionateClobetasol propionate .05 g/mLSprayTopicalAlembic Pharmaceuticals Limited46708-42546708-0425-1246708-0425-59
Clobetasol PropionateClobetasol propionate .5 mg/gOintmentTopicalAlembic Pharmaceuticals Limited46708-46546708-0465-1546708-0465-3046708-0465-45+1 more
Clobetasol PropionateClobetasol propionate .25 mg/gCreamTopicalINA Pharmaceutics Inc74157-71074157-0710-10
Clobetasol PropionateClobetasol propionate .5 mg/gCreamTopicalTorrent Pharmaceuticals Limited13668-56913668-0569-0113668-0569-0213668-0569-04+1 more
Clobetasol PropionateClobetasol propionate .5 mg/mLSprayTopicalMacleods Pharmaceuticals Limited33342-32633342-0326-8733342-0326-88

All 97 Clobetasol Propionate NDCs

Other NDCs under ANDA 215990

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

FDA NDC Directory listings under ANDA 215990
ProductStrengthForm · routeLabelerProduct NDC
Clobetasol PropionateClobetasol propionate .5 mg/gOintmentTopicalA-S Medication Solutions50090-8001
Clobetasol Propionate ANDAclobetasol propionateClobetasol propionate .5 mg/gOintmentTopicalMacleods Pharmaceuticals Limited33342-506

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