What is NDC 70771-1472?

70771-1472 is the product NDC for deferasirox, Deferasirox 180 mg/1 tablet, film coated, listed with the FDA by Zydus Lifesciences Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.

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 deferasirox?

75 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

deferasirox NDC 70771-1472 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1472Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1472Add 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 NDC	11-digit (billing)	Package	Copy
70771-1472-1	7077114720170771147201	100 TABLET, FILM COATED in 1 BOTTLE (70771-1472-1)Marketed from Jun 16, 2020
70771-1472-3	7077114720370771147203	30 TABLET, FILM COATED in 1 BOTTLE (70771-1472-3)Marketed from Jun 16, 2020

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): deferasirox
Generic name (nonproprietary): deferasirox
Active ingredients: Deferasirox — 180 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Zydus Lifesciences LimitedNDC labeler code 70771
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211383
Marketing start: Jun 16, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Cytochrome P450 1A2 Inhibitors (Mechanism)Cytochrome P450 2C8 Inhibitors (Mechanism)Cytochrome P450 3A4 Inducers (Mechanism)Iron Chelating Activity (Mechanism)
Identifiers: Product ID 70771-1472_9e909702-4471-4cd1-8e97-56b38fba9aa6SPL ID 9e909702-4471-4cd1-8e97-56b38fba9aa6SPL set ID fcd2ffe2-c8ba-400b-b7f9-e0e4b3510b98RxCUI 1607784, 1607792, 1607796UNII V8G4MOF2V9
Pharmacologic class: Iron Chelator

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

N470771147201 followed by a unit qualifier and the quantity

Package 70771-1472-01. 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 Nov 26, 2024.

Full label on DailyMed (opens in a new tab)

About NDC 70771-1472

What is NDC 70771-1472?: 70771-1472 is the product NDC for deferasirox, Deferasirox 180 mg/1 tablet, film coated, listed with the FDA by Zydus Lifesciences Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: deferasirox.
What is the active ingredient?: Deferasirox.
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 deferasirox?: 75 other product NDCs are listed under this name. See all deferasirox 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 deferasirox NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Deferasirox	Deferasirox 360 mg/1	TabletOral	AvKARE	73190-052	73190-0052-30
Deferasirox	Deferasirox 90 mg/1	GranuleOral	Aurobindo Pharma Limited	59651-447	59651-0447-30
Deferasirox	Deferasirox 180 mg/1	GranuleOral	Aurobindo Pharma Limited	59651-448	59651-0448-30
Deferasirox	Deferasirox 360 mg/1	GranuleOral	Aurobindo Pharma Limited	59651-449	59651-0449-30
Deferasirox	Deferasirox 125 mg/1	Tablet, For suspensionOral	Teva Pharmaceuticals, Inc.	0480-7011	00480-7011-56
Deferasirox	Deferasirox 250 mg/1	Tablet, For suspensionOral	Teva Pharmaceuticals, Inc.	0480-7012	00480-7012-56
Deferasirox	Deferasirox 500 mg/1	Tablet, For suspensionOral	Teva Pharmaceuticals, Inc.	0480-7013	00480-7013-56
Deferasirox	Deferasirox 360 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-412	59651-0412-30
Deferasirox	Deferasirox 90 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-410	59651-0410-30
Deferasirox	Deferasirox 180 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-411	59651-0411-30

All 76 deferasirox NDCs

Other NDCs under ANDA 211383

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

FDA NDC Directory listings under ANDA 211383
Product	Strength	Form · route	Labeler	Product NDC
deferasirox	Deferasirox 90 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	70710-1275
deferasirox	Deferasirox 180 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	70710-1276
deferasirox	Deferasirox 360 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	70710-1277
deferasirox	Deferasirox 90 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1471
deferasirox	Deferasirox 360 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1473