NDC codes

FDA NDC Directory
Product NDC (as listed)60219-2283Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60219-2283Add 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
60219-2283-1602192283011 BOTTLE in 1 CARTON (60219-2283-1) / 30 TABLET in 1 BOTTLEMarketed from Dec 12, 2025

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)
Deflazacort
Generic name (nonproprietary)
deflazacort
Active ingredients
Deflazacort — 18 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217173
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 60219-2283_bf2296a0-7eb0-484f-b054-3d405c2c1dcaSPL ID bf2296a0-7eb0-484f-b054-3d405c2c1dcaSPL set ID 18518568-a40b-41cb-91ce-44fbb5557971RxCUI 153098, 153880, 1870954, 1870958UNII KR5YZ6AE4BUPC 0360219228313, 0360219228511, 0360219228412, 0360219228214
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N460219228301 followed by a unit qualifier and the quantity

Package 60219-2283-01. 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 .

Indications (excerpt from the label)

Deflazacort tablets are indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients 5 years of age and older. Additional pediatric use information is approved for PTC Therapeutics, Inc.'s Emflaza™ (deflazacort) tablets. However, due to PTC Therapeutics, Inc.'s marketing exclusivity rights, this drug product is not labeled with that information. Deflazacort is a corticosteroid indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients 5 years 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 217173

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

FDA NDC Directory listings under ANDA 217173
ProductStrengthForm · routeLabelerProduct NDC
DeflazacortDeflazacort 6 mg/1TabletOralAmneal Pharmaceuticals NY LLC60219-2282
DeflazacortDeflazacort 30 mg/1TabletOralAmneal Pharmaceuticals NY LLC60219-2284
DeflazacortDeflazacort 36 mg/1TabletOralAmneal Pharmaceuticals NY LLC60219-2285

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