Hydrocortisone Butyrate NDC 72162-2630

NDC codes

FDA NDC Directory

Product NDC (as listed)72162-2630Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72162-2630Add 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	Copy
72162-2630-2	72162263002	1 BOTTLE in 1 CARTON (72162-2630-2) / 59 mL in 1 BOTTLEMarketed from Apr 23, 2026
72162-2630-4	72162263004	1 BOTTLE in 1 CARTON (72162-2630-4) / 118 mL in 1 BOTTLEMarketed from Apr 23, 2026

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 Butyrate
Generic name (nonproprietary): hydrocortisone butyrate
Active ingredients: Hydrocortisone butyrate — 1 mg/mL
Dosage form: Lotion
Route: Topical
Labeler: Bryant Ranch Prepack
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209556
Marketing start: Nov 6, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 72162-2630_ac3f5bf4-9312-4eb1-b70a-c50cd1f9c392SPL ID ac3f5bf4-9312-4eb1-b70a-c50cd1f9c392SPL set ID ce135638-e551-4bb0-bd2b-f97d381a8c7cRxCUI 1370763UNII 05RMF7YPWN
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

N472162263002 followed by a unit qualifier and the quantity

Package 72162-2630-02. 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 Apr 23, 2026.

Indications (excerpt from the label)

Hydrocortisone Butyrate Lotion is indicated for the topical treatment of mild to moderate atopic dermatitis in patients 3 months of age and older. Hydrocortisone Butyrate Lotion is a corticosteroid indicated for the topical treatment of mild to moderate atopic dermatitis in patients 3 months of age and older. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 209556

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

FDA NDC Directory listings under ANDA 209556
Product	Strength	Form · route	Labeler	Product NDC
Evessehydrocortisone butyrate	Hydrocortisone butyrate 1 mg/mL	LotionTopical	Perfero Pharma, Inc.	87143-420
Hydrocortisone Butyrate	Hydrocortisone butyrate 1 mg/mL	LotionTopical	The J. Molner Company LLC	83148-012