NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2954Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2954Add 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
71335-2954-1713352954011 TUBE in 1 CARTON (71335-2954-1) / 30 g in 1 TUBEMarketed from Nov 5, 2025

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
Generic name (nonproprietary)
hydrocortisone
Active ingredients
Hydrocortisone25 mg/g
Dosage form
Cream
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 080706
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 71335-2954_adab8b80-c11c-46da-8116-4b57ec0de5a9SPL ID adab8b80-c11c-46da-8116-4b57ec0de5a9SPL set ID b6808d2d-192c-4d70-a2e8-bf13375c0280RxCUI 310891UNII WI4X0X7BPJ
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

N471335295401 followed by a unit qualifier and the quantity

Package 71335-2954-01. 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)

Other NDCs under ANDA 080706

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

FDA NDC Directory listings under ANDA 080706
ProductStrengthForm · routeLabelerProduct NDC
HydrocortisoneHydrocortisone 10 mg/gCreamTopicalBryant Ranch Prepack72162-1763
HydrocortisoneHydrocortisone 25 mg/gCreamTopicalBryant Ranch Prepack72162-1764
AlacorthydrocortisoneHydrocortisone 10 mg/gCreamTopicalCrown Laboratories0316-0126
AlacorthydrocortisoneHydrocortisone 25 mg/gCreamTopicalCrown Laboratories0316-0128
HydrocortisoneHydrocortisone 25 mg/gCreamTopicalANI Pharmaceuticals, Inc.62559-431
HydrocortisoneHydrocortisone 10 mg/gCreamTopicalANI Pharmaceuticals, Inc.62559-430
HydrocortisoneHydrocortisone 10 mg/gCreamTopicalCrown Laboratories0316-0186
HydrocortisoneHydrocortisone 25 mg/gCreamTopicalCrown Laboratories0316-0193
HydrocortisoneHydrocortisone 25 mg/gCreamTopicalSportpharm LLC85766-085
HydrocortisoneHydrocortisone 25 mg/gCreamTopicalPreferred Pharmaceuticals, Inc.68788-8302
HydrocortisoneHydrocortisone 25 mg/gCreamTopicalA-S Medication Solutions50090-2452
HydrocortisoneHydrocortisone 10 mg/gCreamTopicalBryant Ranch Prepack63629-1951
HydrocortisoneHydrocortisone 25 mg/gCreamTopicalBryant Ranch Prepack63629-1952

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