What is NDC 71205-364?

71205-364 is the product NDC for Betamethasone Valerate, Betamethasone valerate 1.2 mg/g ointment, listed with the FDA by Proficient Rx LP. It has 1 package NDC, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 71205. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Betamethasone Valerate NDC 71205-364

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-364Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0364Add 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
71205-364-15	7120503641571205036415	1 TUBE in 1 CARTON (71205-364-15) / 15 g in 1 TUBEMarketed from Nov 20, 2019

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 — 1.2 mg/g
Dosage form: Ointment
Route: Topical
Labeler: Proficient Rx LPNDC labeler code 71205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 070069
Marketing start: Dec 19, 1985
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 71205-364_e104fc1b-b0dd-4452-84cb-0b90527f25f8SPL ID e104fc1b-b0dd-4452-84cb-0b90527f25f8SPL set ID 2a64b65b-8a49-45ea-9464-2269751c075cRxCUI 197409UNII 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

N471205036415 followed by a unit qualifier and the quantity

Package 71205-0364-15. 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 1, 2021.

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 71205-364

What is NDC 71205-364?: 71205-364 is the product NDC for Betamethasone Valerate, Betamethasone valerate 1.2 mg/g ointment, listed with the FDA by Proficient Rx LP. 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?: Proficient Rx LP, NDC labeler code 71205. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Betamethasone valerate	Betamethasone valerate 1.2 mg/g	Aerosol, FoamTopical	Alembic Pharmaceuticals Limited	46708-708	46708-0708-3146708-0708-50
Betamethasone valerate	Betamethasone valerate 1.2 mg/g	Aerosol, FoamTopical	Alembic Pharmaceuticals Inc.	62332-708	62332-0708-3162332-0708-50
Betamethasone Valerate	Betamethasone valerate 1 mg/g	OintmentTopical	Preferred Pharmaceuticals Inc.	68788-8496	68788-8496-0168788-8496-04
Betamethasone Valerate	Betamethasone valerate 1 mg/g	CreamTopical	Preferred Pharmaceuticals Inc.	68788-8450	68788-8450-0168788-8450-04
Betamethasone Valeratebetamethasone valerate foam	Betamethasone valerate 1.2 mg/g	Aerosol, FoamTopical	Xiromed, LLC.	70700-141	70700-0141-1970700-0141-20
Betamethasone Valerate	Betamethasone valerate 1.2 mg/g	Aerosol, FoamTopical	Sun Pharmaceutical Industries, Inc.	51672-4188	51672-4188-0351672-4188-07
Betamethasone Valerate	Betamethasone valerate 1.2 mg/g	Aerosol, FoamTopical	Padagis Israel Pharmaceuticals Ltd	45802-053	45802-0053-0145802-0053-02
Betamethasone Valerate	Betamethasone valerate 1 mg/g	CreamTopical	A-S Medication Solutions	50090-1647	50090-1647-00
Betamethasone Valerate	Betamethasone valerate 1 mg/g	CreamTopical	A-S Medication Solutions	50090-3134	50090-3134-01
Betamethasone Valerate	Betamethasone valerate 1 mg/g	CreamTopical	Sun Pharmaceutical Industries, Inc.	51672-1269	51672-1269-0151672-1269-06

All 22 Betamethasone Valerate NDCs

Other NDCs under ANDA 070069

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

FDA NDC Directory listings under ANDA 070069
Product	Strength	Form · route	Labeler	Product NDC
Betamethasone Valerate	Betamethasone valerate 1.2 mg/g	OintmentTopical	Cosette Pharmaceuticals, Inc.	0713-0327