NDC codes

FDA NDC Directory
Product NDC (as listed)68462-625Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68462-0625Add 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
68462-625-276846206252750 g in 1 CAN (68462-625-27)Marketed from Sep 9, 2019
68462-625-9468462062594100 g in 1 CAN (68462-625-94)Marketed from Sep 9, 2019

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
Aerosol, Foam
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211450
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 68462-625_5dad350f-062c-4799-9cdb-1272c56ccda7SPL ID 5dad350f-062c-4799-9cdb-1272c56ccda7SPL set ID 6a3ad15e-2874-40d0-9e69-105b369c8cfcRxCUI 1992273UNII 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

N468462062527 followed by a unit qualifier and the quantity

Package 68462-0625-27. 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)

Clobetasol propionate emulsion foam is indicated for the treatment of inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients 12 years and older. Clobetasol propionate emulsion foam is a corticosteroid indicated for the treatment of inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients aged 12 years and older. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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