NDC codes

FDA NDC Directory
Product NDC (as listed)70377-188Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70377-0188Add 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
70377-188-21703770188211 BOTTLE in 1 CARTON (70377-188-21) / 13 mL in 1 BOTTLEMarketed from Sep 25, 2026

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 oral
Active ingredients
Deflazacort — 22.75 mg/mL
Dosage form
Suspension
Route
Oral
Labeler
Biocon Pharma Inc.NDC labeler code 70377
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 220709
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 70377-188_3f0a59d0-17a9-264b-9081-b858e4198d98SPL ID 3f0a59d0-17a9-264b-9081-b858e4198d98
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

N470377018821 followed by a unit qualifier and the quantity

Package 70377-0188-21. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70377-188

What is NDC 70377-188?
70377-188 is the product NDC for Deflazacort Oral Suspension (deflazacort oral), Deflazacort 22.75 mg/mL suspension, listed with the FDA by Biocon Pharma Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Deflazacort Oral Suspension (Deflazacort Oral).
What is the active ingredient?
Deflazacort.
Who is the labeler?
Biocon Pharma Inc., NDC labeler code 70377. 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/mLSuspensionOralSun Pharmaceutical Industries, Inc.57664-99357664-0993-01
Deflazacort Oral SuspensiondeflazacortDeflazacort 22.75 mg/mLSuspensionOralZydus Pharmaceuticals (USA) Inc.70710-200770710-2007-03
Deflazacort Oral SuspensiondeflazacortDeflazacort 22.75 mg/mLSuspensionOralDoppel Farmaceutici S.r.l.81806-20081806-0200-73
Deflazacort Oral Suspensiondeflazacort oralDeflazacort 22.75 mg/mLSuspensionOralCranbury Pharmaceuticals, LLC27808-24927808-0249-01

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