NDC codes

FDA NDC Directory
Product NDC (as listed)68180-947Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68180-0947Add 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
68180-947-01681800947011 TUBE in 1 CARTON (68180-947-01) / 15 g in 1 TUBEMarketed from Mar 19, 2020
68180-947-02681800947021 TUBE in 1 CARTON (68180-947-02) / 50 g in 1 TUBEMarketed from Mar 19, 2020

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)
Betamethasone dipropionate
Generic name (nonproprietary)
betamethasone dipropionate
Active ingredients
Betamethasone dipropionate — .5 mg/g
Dosage form
Ointment, Augmented
Route
Topical
Labeler
Lupin Pharmaceuticals, Inc.NDC labeler code 68180
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209106
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 68180-947_fb870496-75f5-4f2a-a156-2552d9c13e7fSPL ID fb870496-75f5-4f2a-a156-2552d9c13e7fSPL set ID 216d5b7f-4236-4882-b899-be17cb1a1584RxCUI 848180UNII 826Y60901UUPC 0368180947028
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

N468180094701 followed by a unit qualifier and the quantity

Package 68180-0947-01. 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)

Betamethasone dipropionate ointment USP (augmented) is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients 13 years of age or older. Betamethasone dipropionate ointment USP (augmented) is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients 13 years of age and older. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68180-947

What is NDC 68180-947?
68180-947 is the product NDC for Betamethasone dipropionate, Betamethasone dipropionate .5 mg/g ointment, augmented, listed with the FDA by Lupin Pharmaceuticals, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Betamethasone dipropionate.
What is the active ingredient?
Betamethasone dipropionate.
Who is the labeler?
Lupin Pharmaceuticals, Inc., NDC labeler code 68180. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Betamethasone dipropionate?
54 other product NDCs are listed under this name. See all 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 Betamethasone dipropionate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gCreamTopicalAurobindo Pharma Limited59651-89159651-0891-1459651-0891-46
Betamethasone DipropionateBetamethasone dipropionate .5 mg/mLLotion, AugmentedTopicalEncube Ethicals, Inc.21922-10421922-0104-0121922-0104-21
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gOintment, AugmentedTopicalBurel Pharmaceuticals, LLC35573-10735573-0107-1535573-0107-49
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gCreamTopicalREMEDYREPACK INC.70518-418770518-4187-00
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gOintment, AugmentedTopicalAurobindo Pharma Limited59651-69959651-0699-1459651-0699-4659651-0699-50
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gOintmentTopicalPadagis Israel Pharmaceuticals Ltd45802-50545802-0505-1445802-0505-84
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gOintmentTopicalBryant Ranch Prepack63629-932363629-9323-01
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gOintmentTopicalBryant Ranch Prepack63629-932463629-9324-01
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gOintmentTopicalBryant Ranch Prepack71335-271571335-2715-01
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gOintmentTopicalBryant Ranch Prepack72162-141572162-1415-0272162-1415-04

All 55 Betamethasone dipropionate NDCs

Other NDCs under ANDA 209106

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

FDA NDC Directory listings under ANDA 209106
ProductStrengthForm · routeLabelerProduct NDC
Betamethasone dipropionateBetamethasone dipropionate .5 mg/gOintment, AugmentedTopicalA-S Medication Solutions50090-6787

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