NDC codes

FDA NDC Directory
Product NDC (as listed)63629-2520Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63629-2520Add 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
63629-2520-1636292520011 TUBE in 1 CARTON (63629-2520-1) / 60 g in 1 TUBEMarketed from Jan 30, 2020

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

Generic name (nonproprietary)
calcipotriene, betamethasone dipropionate
Active ingredients
Calcipotriene — 50 ug/gBetamethasone dipropionate — .643 mg/g
Dosage form
Ointment
Route
Topical
Labeler
Bryant Ranch PrepackNDC labeler code 63629
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 200174
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)Vitamin D (Chemical structure)
Identifiers
Product ID 63629-2520_ea65f651-7e10-4b2e-af33-fd75351b3b8cSPL ID ea65f651-7e10-4b2e-af33-fd75351b3b8cSPL set ID 174c5378-f2b9-4e9e-931a-4123137be62dRxCUI 388525UNII 143NQ3779B, 826Y60901U
Pharmacologic class
Corticosteroid; Vitamin D Analog

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

N463629252001 followed by a unit qualifier and the quantity

Package 63629-2520-01. 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)

Calcipotriene and Betamethasone Dipropionate Ointment is indicated for the topical treatment of plaque psoriasis in patients 12 years of age and older. Calcipotriene and Betamethasone Dipropionate Ointment is a vitamin D analogue and corticosteroid combination product indicated for the topical treatment of plaque psoriasis in patients 12 years of age and older.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63629-2520

What is NDC 63629-2520?
63629-2520 is the product NDC for Calcipotriene and Betamethasone Dipropionate, Calcipotriene 50 ug/g; Betamethasone dipropionate .643 mg/g ointment, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Calcipotriene and Betamethasone Dipropionate (Calcipotriene, Betamethasone Dipropionate).
What is the active ingredient?
Calcipotriene, Betamethasone dipropionate.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 63629. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Calcipotriene and Betamethasone Dipropionate?
6 other product NDCs are listed under this name. See all Calcipotriene and Betamethasone Dipropionate 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 Calcipotriene and Betamethasone Dipropionate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
calcipotriene and betamethasone dipropionateBetamethasone dipropionate .5 mg/g; Calcipotriene 50 ug/gSuspensionTopicalCosette Pharmaceuticals, Inc.0713-084800713-0848-6000713-0848-92
Calcipotriene and Betamethasone DipropionateCalcipotriene 50 ug/g; Betamethasone dipropionate 50 mg/gSuspensionTopicalSun Pharmaceutical Industries, Inc.51672-140251672-1402-0451672-1402-08
Calcipotriene and Betamethasone Dipropionatecalcipotriene, betamethasone dipropionateCalcipotriene 50 ug/g; Betamethasone dipropionate .643 mg/gOintmentTopicalPadagis Israel Pharmaceuticals Ltd45802-81645802-0816-0145802-0816-96
Calcipotriene and Betamethasone Dipropionatecalcipotriene, betamethasone dipropionateCalcipotriene 50 ug/g; Betamethasone dipropionate .643 mg/gOintmentTopicalBryant Ranch Prepack63629-861763629-8617-01
Calcipotriene and Betamethasone Dipropionatecalcipotriene, betamethasone dipropionateCalcipotriene 50 ug/g; Betamethasone dipropionate .643 mg/gOintmentTopicalBryant Ranch Prepack72162-142872162-1428-0172162-1428-06
Calcipotriene and Betamethasone DipropionateCalcipotriene monohydrate 50 ug/g; Betamethasone dipropionate .5 mg/gOintmentTopicalPrasco Laboratories66993-93866993-0938-6166993-0938-65

Other NDCs under ANDA 200174

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

FDA NDC Directory listings under ANDA 200174
ProductStrengthForm · routeLabelerProduct NDC
Calcipotriene and Betamethasone Dipropionatecalcipotriene, betamethasone dipropionateCalcipotriene 50 ug/g; Betamethasone dipropionate .643 mg/gOintmentTopicalPadagis Israel Pharmaceuticals Ltd45802-816
Calcipotriene and Betamethasone Dipropionatecalcipotriene, betamethasone dipropionateCalcipotriene 50 ug/g; Betamethasone dipropionate .643 mg/gOintmentTopicalBryant Ranch Prepack63629-8617
Calcipotriene and Betamethasone Dipropionatecalcipotriene, betamethasone dipropionateCalcipotriene 50 ug/g; Betamethasone dipropionate .643 mg/gOintmentTopicalBryant Ranch Prepack72162-1428

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