NDC codes

FDA NDC Directory
Product NDC (as listed)68071-4278Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-4278Add 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
68071-4278-5680714278056807142780515 g in 1 BOX (68071-4278-5)Marketed from Feb 8, 2018

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
NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 072041
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 68071-4278_1a3dc88f-20dc-241c-e063-6294a90aa423SPL ID 1a3dc88f-20dc-241c-e063-6294a90aa423SPL set ID 64badc1a-8922-c6e3-e053-2991aa0a8b1cRxCUI 197407UNII 9IFA5XM7R2UPC 0368071427851
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

N468071427805 followed by a unit qualifier and the quantity

Package 68071-4278-05. 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 68071-4278

What is NDC 68071-4278?
68071-4278 is the product NDC for Betamethasone Valerate, Betamethasone valerate 1 mg/g cream, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 1 package NDC, 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?
NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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 1 mg/gCreamTopicalPreferred Pharmaceuticals Inc.68788-845068788-8450-0168788-8450-04
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

All 22 Betamethasone Valerate NDCs

Other NDCs under ANDA 072041

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

FDA NDC Directory listings under ANDA 072041
ProductStrengthForm · routeLabelerProduct NDC
Betamethasone ValerateBetamethasone valerate 1 mg/gCreamTopicalA-S Medication Solutions50090-1647
Betamethasone ValerateBetamethasone valerate 1 mg/gCreamTopicalA-S Medication Solutions50090-3134
Betamethasone ValerateBetamethasone valerate 1 mg/gCreamTopicalSun Pharmaceutical Industries, Inc.51672-1269
Betamethasone ValerateBetamethasone valerate 1 mg/gCreamTopicalPreferred Pharmaceuticals, Inc.68788-7451

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