What is NDC 51672-1290?

51672-1290 is the product NDC for Hydrocortisone Valerate, Hydrocortisone valerate 2 mg/g cream, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Hydrocortisone Valerate?

5 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Hydrocortisone Valerate NDC 51672-1290

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-1290Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-1290Add 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 NDC	11-digit (billing)	Package
51672-1290-1	5167212900151672129001	1 TUBE in 1 CARTON (51672-1290-1) / 15 g in 1 TUBEMarketed from Aug 25, 1998
51672-1290-3	5167212900351672129003	1 TUBE in 1 CARTON (51672-1290-3) / 60 g in 1 TUBEMarketed from Aug 25, 1998
51672-1290-6	5167212900651672129006	1 TUBE in 1 CARTON (51672-1290-6) / 45 g in 1 TUBEMarketed from Aug 25, 1998

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): Hydrocortisone Valerate
Generic name (nonproprietary): hydrocortisone valerate
Active ingredients: Hydrocortisone valerate — 2 mg/g
Dosage form: Cream
Route: Topical
Labeler: Sun Pharmaceutical Industries, Inc.NDC labeler code 51672
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075042
Marketing start: Aug 25, 1998
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 51672-1290_39628349-b388-4030-e063-6394a90a6ce9SPL ID 39628349-b388-4030-e063-6394a90a6ce9SPL set ID a9011d6f-6808-48a7-ab6b-df8d40540570RxCUI 1370750, 1370754UNII 68717P8FUZ
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

N451672129001 followed by a unit qualifier and the quantity

Package 51672-1290-01. 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 Jul 7, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hydrocortisone valerate cream, 0.2% and hydrocortisone valerate ointment, 0.2% are medium potency corticosteroids indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses in adult patients.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51672-1290

What is NDC 51672-1290?: 51672-1290 is the product NDC for Hydrocortisone Valerate, Hydrocortisone valerate 2 mg/g cream, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Hydrocortisone Valerate.
What is the active ingredient?: Hydrocortisone valerate.
Who is the labeler?: Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hydrocortisone Valerate?: 5 other product NDCs are listed under this name. See all Hydrocortisone 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 Hydrocortisone Valerate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Hydrocortisone Valerate	Hydrocortisone valerate 2 mg/g	CreamTopical	Cosette Pharmaceuticals, Inc.	0713-0720	00713-0720-1500713-0720-3700713-0720-60
Hydrocortisone Valerate	Hydrocortisone valerate 2 mg/g	OintmentTopical	Cosette Pharmaceuticals, Inc.	0713-0560	00713-0560-1500713-0560-3700713-0560-60
Hydrocortisone Valerate	Hydrocortisone valerate 2 mg/g	CreamTopical	Lupin Pharmaceuticals, Inc.	68180-954	68180-0954-0168180-0954-0268180-0954-03
Hydrocortisone Valerate	Hydrocortisone valerate 2 mg/g	OintmentTopical	Glenmark Pharmaceuticals Inc., USA	68462-836	68462-0836-1768462-0836-4768462-0836-65
Hydrocortisone Valerate	Hydrocortisone valerate 2 mg/g	OintmentTopical	Sun Pharmaceutical Industries, Inc.	51672-1292	51672-1292-0151672-1292-0351672-1292-06