Clobetasol Propionate NDC 70771-1209

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1209Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1209Add 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
70771-1209-1	70771120901	1 TUBE in 1 CARTON (70771-1209-1) / 15 g in 1 TUBEMarketed from Mar 22, 2018
70771-1209-2	70771120902	1 TUBE in 1 CARTON (70771-1209-2) / 30 g in 1 TUBEMarketed from Mar 22, 2018
70771-1209-3	70771120903	1 TUBE in 1 CARTON (70771-1209-3) / 60 g in 1 TUBEMarketed from Mar 22, 2018
70771-1209-4	70771120904	1 TUBE in 1 CARTON (70771-1209-4) / 45 g in 1 TUBEMarketed from Mar 22, 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): Clobetasol Propionate
Generic name (nonproprietary): clobetasol propionate
Active ingredients: Clobetasol propionate — .5 mg/g
Dosage form: Ointment
Route: Topical
Labeler: Zydus Lifesciences Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210199
Marketing start: Mar 22, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 70771-1209_b9149016-e029-4b79-90f1-58670ba7df3bSPL ID b9149016-e029-4b79-90f1-58670ba7df3bSPL set ID 30f4c173-189d-4b29-8d7d-e82e5c0743cfRxCUI 861448UNII 779619577M
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

N470771120901 followed by a unit qualifier and the quantity

Package 70771-1209-01. 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 Nov 26, 2024.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 210199

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

FDA NDC Directory listings under ANDA 210199
Product	Strength	Form · route	Labeler	Product NDC
Clobetasol Propionate	Clobetasol propionate .5 mg/g	OintmentTopical	Zydus Pharmaceuticals USA Inc.	70710-1401