Fluocinonide NDC 70700-146

NDC codes

FDA NDC Directory

Product NDC (as listed)70700-146Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70700-0146Add 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
70700-146-15	70700014615	1 TUBE in 1 CARTON (70700-146-15) / 15 g in 1 TUBEMarketed from Dec 9, 2019
70700-146-16	70700014616	1 TUBE in 1 CARTON (70700-146-16) / 30 g in 1 TUBEMarketed from Dec 9, 2019
70700-146-17	70700014617	1 TUBE in 1 CARTON (70700-146-17) / 60 g in 1 TUBEMarketed from Dec 9, 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): Fluocinonide
Generic name (nonproprietary): fluocinonide
Active ingredients: Fluocinonide — .05 mg/g
Dosage form: Ointment
Route: Topical
Labeler: Xiromed LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212976
Marketing start: Dec 9, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 70700-146_2bfc0a7d-82bb-11d0-8ea7-c2d2a9c836acSPL ID 2bfc0a7d-82bb-11d0-8ea7-c2d2a9c836acSPL set ID d96cc4fd-abd3-1ce1-ac63-5d68a8332eccUNII 2W4A77YPANUPC 0370700146170, 0370700146156, 0370700146163
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

N470700014615 followed by a unit qualifier and the quantity

Package 70700-0146-15. 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 Jan 13, 2020.

Indications (excerpt from the label)

INDICATIONS AND USAGE Fluocinonide Ointment is 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 212976

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

FDA NDC Directory listings under ANDA 212976
Product	Strength	Form · route	Labeler	Product NDC
Fluocinonide	Fluocinonide .05 mg/g	OintmentTopical	Bryant Ranch Prepack	63629-2337
Fluocinonide	Fluocinonide .05 mg/g	OintmentTopical	Bryant Ranch Prepack	63629-2338
Fluocinonide	Fluocinonide .05 mg/g	OintmentTopical	Bryant Ranch Prepack	63629-2339
Fluocinonide	Fluocinonide .05 mg/g	OintmentTopical	Bryant Ranch Prepack	72162-1972