NDC codes

FDA NDC Directory
Product NDC (as listed)72162-1271Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-1271Add 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
72162-1271-6721621271061 BOTTLE in 1 CARTON (72162-1271-6) / 60 mL in 1 BOTTLEMarketed from Mar 20, 2019

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)
Fluocinolone Acetonide Topical Solution USP, 0.01%
Generic name (nonproprietary)
fluocinolone acetonide topical solution usp, 0.01%
Active ingredients
Fluocinolone acetonide — .1 mg/mL
Dosage form
Solution
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209913
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 72162-1271_10500bf6-853d-43bc-a231-07f349923a84SPL ID 10500bf6-853d-43bc-a231-07f349923a84SPL set ID 3fa4d5db-b17f-44dc-aa6a-50934d42c68dRxCUI 1191310UNII 0CD5FD6S2M
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

N472162127106 followed by a unit qualifier and the quantity

Package 72162-1271-06. 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 Fluocinolone Acetonide Topical Solution USP, 0.01% 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 209913

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

FDA NDC Directory listings under ANDA 209913
ProductStrengthForm · routeLabelerProduct NDC
Fluocinolone Acetonide Topical Solution USP, 0.01%Fluocinolone acetonide .1 mg/mLSolutionTopicalEncube Ethicals, Inc.21922-003
Fluocinolone Acetonide Topical Solution USP, 0.01%Fluocinolone acetonide .1 mg/mLSolutionTopicalBryant Ranch Prepack63629-9584

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