NDC codes

FDA NDC Directory
Product NDC (as listed)40032-096Labeler and product segments. Claims need a package NDC.
Product NDC at billing width40032-0096Add 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
40032-096-6040032009660400320096601 TUBE in 1 CARTON (40032-096-60) / 15 g in 1 TUBEMarketed from Nov 25, 2016
40032-096-6140032009661400320096611 TUBE in 1 CARTON (40032-096-61) / 30 g in 1 TUBEMarketed from Nov 25, 2016
40032-096-6240032009662400320096621 TUBE in 1 CARTON (40032-096-62) / 60 g in 1 TUBEMarketed from Nov 25, 2016

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
Novel Laboratories, Inc.NDC labeler code 40032
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208841
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 40032-096_3853a6ab-db3f-4b76-b323-d769289a33ffSPL ID 3853a6ab-db3f-4b76-b323-d769289a33ffSPL set ID c7c03887-f84a-417e-a8f1-5272f530d0bbRxCUI 861448UNII 779619577MUPC 0340032096603
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

N440032009660 followed by a unit qualifier and the quantity

Package 40032-0096-60. 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 USP is a super-high potency corticosteroid formulation 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 40032-096

What is NDC 40032-096?
40032-096 is the product NDC for clobetasol propionate, Clobetasol propionate .5 mg/g ointment, listed with the FDA by Novel Laboratories, Inc.. It has 3 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?
Novel Laboratories, Inc., NDC labeler code 40032. 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/gOintmentTopicalNorthStar RxLLC72603-85572603-0855-0172603-0855-0272603-0855-03+1 more
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

All 97 clobetasol propionate NDCs

Other NDCs under ANDA 208841

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

FDA NDC Directory listings under ANDA 208841
ProductStrengthForm · routeLabelerProduct NDC
clobetasol propionateClobetasol propionate .5 mg/gOintmentTopicalLupin Pharmaceuticals,Inc.43386-096

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