NDC codes

FDA NDC Directory
Product NDC (as listed)81806-200Labeler and product segments. Claims need a package NDC.
Product NDC at billing width81806-0200Add 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
81806-200-7381806020073818060200731 BOTTLE in 1 CARTON (81806-200-73) / 13 mL in 1 BOTTLEMarketed from Oct 23, 2025

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)
Deflazacort Oral Suspension
Generic name (nonproprietary)
deflazacort
Active ingredients
Deflazacort — 22.75 mg/mL
Dosage form
Suspension
Route
Oral
Labeler
Doppel Farmaceutici S.r.l.NDC labeler code 81806
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 220042
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 81806-200_57c38c16-099f-a6e0-e063-6294a90a2304SPL ID 57c38c16-099f-a6e0-e063-6294a90a2304SPL set ID 40a833a4-e029-a99e-e063-6394a90afd50RxCUI 1870964UNII KR5YZ6AE4BUPC 0370710200732
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

N481806020073 followed by a unit qualifier and the quantity

Package 81806-0200-73. 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 oral suspension is indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients 2 years of age and older. Deflazacort oral suspension is a corticosteroid indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients 2 years of age and older ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 81806-200

What is NDC 81806-200?
81806-200 is the product NDC for Deflazacort Oral Suspension (deflazacort), Deflazacort 22.75 mg/mL suspension, listed with the FDA by Doppel Farmaceutici S.r.l.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Deflazacort Oral Suspension (Deflazacort).
What is the active ingredient?
Deflazacort.
Who is the labeler?
Doppel Farmaceutici S.r.l., NDC labeler code 81806. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Deflazacort Oral Suspension?
4 other product NDCs are listed under this name. See all Deflazacort Oral Suspension 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 Deflazacort Oral Suspension NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Deflazacort Oral Suspensiondeflazacort oralDeflazacort 22.75 mg/mLSuspensionOralBiocon Pharma Inc.70377-18870377-0188-21
Deflazacort Oral Suspensiondeflazacort oralDeflazacort 22.75 mg/mLSuspensionOralSun Pharmaceutical Industries, Inc.57664-99357664-0993-01
Deflazacort Oral SuspensiondeflazacortDeflazacort 22.75 mg/mLSuspensionOralZydus Pharmaceuticals (USA) Inc.70710-200770710-2007-03
Deflazacort Oral Suspensiondeflazacort oralDeflazacort 22.75 mg/mLSuspensionOralCranbury Pharmaceuticals, LLC27808-24927808-0249-01

Other NDCs under ANDA 220042

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

FDA NDC Directory listings under ANDA 220042
ProductStrengthForm · routeLabelerProduct NDC
Deflazacort Oral SuspensiondeflazacortDeflazacort 22.75 mg/mLSuspensionOralZydus Pharmaceuticals (USA) Inc.70710-2007
JAYTHARI Oral SuspensiondeflazacortDeflazacort 22.75 mg/mLSuspensionOralZydus Pharmaceuticals (USA) Inc.70710-2131
JAYTHARI Oral SuspensiondeflazacortDeflazacort 22.75 mg/mLSuspensionOralDoppel Farmaceutici S.r.l.81806-213

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