NDC codes

FDA NDC Directory
Product NDC (as listed)68788-9219Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68788-9219Add 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
68788-9219-1687889219011 TUBE in 1 CARTON (68788-9219-1) / 15 g in 1 TUBEMarketed from Sep 19, 2014

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

Brand name (proprietary)
Betamethasone Dipropionate
Generic name (nonproprietary)
betamethasone dipropionate
Active ingredients
Betamethasone dipropionate — .5 mg/g
Dosage form
Cream
Route
Topical
Labeler
Preferred Pharmaceuticals, Inc.NDC labeler code 68788
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076592
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 68788-9219_1b8a928c-7c86-4359-9b9d-a000809cf275SPL ID 1b8a928c-7c86-4359-9b9d-a000809cf275SPL set ID 5683885d-461c-4e7e-bbe8-dc231d706192RxCUI 848176UNII 826Y60901U
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

N468788921901 followed by a unit qualifier and the quantity

Package 68788-9219-01. 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 Cream USP (Augmented), 0.05% 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 Cream USP (Augmented), 0.05% 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.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68788-9219

What is NDC 68788-9219?
68788-9219 is the product NDC for Betamethasone Dipropionate, Betamethasone dipropionate .5 mg/g cream, listed with the FDA by Preferred Pharmaceuticals, Inc.. It has 1 package NDC, 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?
Preferred Pharmaceuticals, Inc., NDC labeler code 68788. 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/gOintmentTopicalBryant Ranch Prepack71335-271571335-2715-01
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/gOintmentTopicalPadagis Israel Pharmaceuticals Ltd45802-50545802-0505-1445802-0505-84
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gOintmentTopicalBryant Ranch Prepack72162-141572162-1415-0272162-1415-04

All 55 Betamethasone Dipropionate NDCs

Other NDCs under ANDA 076592

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

FDA NDC Directory listings under ANDA 076592
ProductStrengthForm · routeLabelerProduct NDC
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gCreamTopicalBryant Ranch Prepack63629-8613
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gCreamTopicalBryant Ranch Prepack63629-8614
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gCreamTopicalPadagis Israel Pharmaceuticals Ltd45802-376
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gCreamTopicalNuCare Pharmaceuticals,Inc.68071-4814
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gCreamTopicalProficient Rx LP71205-275
Betamethasone DipropionateBetamethasone dipropionate .5 mg/gCreamTopicalBryant Ranch Prepack72162-1405

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