NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1701Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1701Add 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
70771-1701-170771170101100 TABLET in 1 BOTTLE (70771-1701-1)Marketed from Apr 15, 2024

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)
Dexamethasone
Generic name (nonproprietary)
dexamethasone
Active ingredients
Dexamethasone — 2 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Zydus Lifesciences LimitedNDC labeler code 70771
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216283
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 70771-1701_6a9c20d5-8b08-4b8e-b422-705383158851SPL ID 6a9c20d5-8b08-4b8e-b422-705383158851SPL set ID 1e84a609-22a0-41b9-83a0-c45019c8cf9aRxCUI 197581UNII 7S5I7G3JQL
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

N470771170101 followed by a unit qualifier and the quantity

Package 70771-1701-01. 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 .

Full label on DailyMed (opens in a new tab)

About NDC 70771-1701

What is NDC 70771-1701?
70771-1701 is the product NDC for Dexamethasone, Dexamethasone 2 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Dexamethasone.
What is the active ingredient?
Dexamethasone.
Who is the labeler?
Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dexamethasone?
135 other product NDCs are listed under this name. See all Dexamethasone 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 Dexamethasone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
DexamethasoneDexamethasone 4 mg/1TabletOralPreferred Pharmaceuticals Inc68788-411368788-4113-0168788-4113-0368788-4113-05+1 more
DexamethasoneDexamethasone .5 mg/1TabletOralREMEDYREPACK INC.70518-466970518-4669-00
DexamethasoneDexamethasone .25 mg/1TabletOralPangea Pharmaceuticals, LLC81279-11781279-0117-60
DexamethasoneDexamethasone .25 mg/1TabletOralPangea Pharmaceuticals, LLC81279-11781279-0117-88
DexamethasoneDexamethasone .5 mg/5mLElixirOralANI Pharmaceuticals, Inc.70954-87270954-0872-10
DexamethasoneDexamethasone 4 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-53472789-0534-0172789-0534-2872789-0534-95
DexamethasoneDexamethasone .5 mg/5mLElixirOralKanchan Healthcare Inc85742-00485742-0004-03
DexamethasoneDexamethasone .5 mg/5mLElixirOralBryant Ranch Prepack72162-260072162-2600-02
DexamethasoneDexamethasone .75 mg/1TabletOralAdvagen Pharma Ltd.72888-23672888-0236-01
DexamethasoneDexamethasone .5 mg/1TabletOralAdvagen Pharma Ltd.72888-23572888-0235-01

All 136 Dexamethasone NDCs

Other NDCs under ANDA 216283

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

FDA NDC Directory listings under ANDA 216283
ProductStrengthForm · routeLabelerProduct NDC
DexamethasoneDexamethasone 2 mg/1TabletOralViona Pharmaceuticals Inc72578-167

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