NDC codes

FDA NDC Directory
Product NDC (as listed)68788-8450Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68788-8450Add 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
68788-8450-16878884500115 g in 1 TUBE (68788-8450-1)Marketed from May 26, 2023
68788-8450-46878884500445 g in 1 TUBE (68788-8450-4)Marketed from May 26, 2023

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 Valerate
Generic name (nonproprietary)
betamethasone valerate
Active ingredients
Betamethasone valerate — 1 mg/g
Dosage form
Cream
Route
Topical
Labeler
Preferred Pharmaceuticals Inc.NDC labeler code 68788
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 018861
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 68788-8450_3eeca6c3-ceab-4edf-a799-fdec16cbed8aSPL ID 3eeca6c3-ceab-4edf-a799-fdec16cbed8aSPL set ID 985d1f62-4bff-4bf1-b7c7-96cb456ef83dRxCUI 197407UNII 9IFA5XM7R2
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

N468788845001 followed by a unit qualifier and the quantity

Package 68788-8450-01. 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)

INDICATIONS AND USAGE: Topical corticosteroids are indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68788-8450

What is NDC 68788-8450?
68788-8450 is the product NDC for Betamethasone Valerate, Betamethasone valerate 1 mg/g cream, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Betamethasone Valerate.
What is the active ingredient?
Betamethasone valerate.
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 Valerate?
21 other product NDCs are listed under this name. See all Betamethasone Valerate 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 Valerate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Betamethasone valerateBetamethasone valerate 1.2 mg/gAerosol, FoamTopicalAlembic Pharmaceuticals Limited46708-70846708-0708-3146708-0708-50
Betamethasone valerateBetamethasone valerate 1.2 mg/gAerosol, FoamTopicalAlembic Pharmaceuticals Inc.62332-70862332-0708-3162332-0708-50
Betamethasone ValerateBetamethasone valerate 1 mg/gOintmentTopicalPreferred Pharmaceuticals Inc.68788-849668788-8496-0168788-8496-04
Betamethasone Valeratebetamethasone valerate foamBetamethasone valerate 1.2 mg/gAerosol, FoamTopicalXiromed, LLC.70700-14170700-0141-1970700-0141-20
Betamethasone ValerateBetamethasone valerate 1.2 mg/gAerosol, FoamTopicalSun Pharmaceutical Industries, Inc.51672-418851672-4188-0351672-4188-07
Betamethasone ValerateBetamethasone valerate 1.2 mg/gAerosol, FoamTopicalPadagis Israel Pharmaceuticals Ltd45802-05345802-0053-0145802-0053-02
Betamethasone ValerateBetamethasone valerate 1 mg/gCreamTopicalA-S Medication Solutions50090-164750090-1647-00
Betamethasone ValerateBetamethasone valerate 1 mg/gCreamTopicalA-S Medication Solutions50090-313450090-3134-01
Betamethasone ValerateBetamethasone valerate 1 mg/gCreamTopicalSun Pharmaceutical Industries, Inc.51672-126951672-1269-0151672-1269-06
Betamethasone ValerateBetamethasone valerate 1 mg/gCreamTopicalNuCare Pharmaceuticals,Inc.68071-427868071-4278-05

All 22 Betamethasone Valerate NDCs

Other NDCs under NDA 018861

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

FDA NDC Directory listings under NDA 018861
ProductStrengthForm · routeLabelerProduct NDC
Betamethasone ValerateBetamethasone valerate 1 mg/gCreamTopicalE. Fougera & Co. a division of Fougera Pharmaceuticals, LLC0168-0040
Betamethasone ValerateBetamethasone valerate 1 mg/gCreamTopicalProficient Rx LP71205-040

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