NDC codes

FDA NDC Directory
Product NDC (as listed)0093-8231Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00093-8231Add 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
0093-8231-28000938231280009382312828 CAPSULE in 1 BOTTLE (0093-8231-28)Marketed from Dec 22, 2021

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Sunitinib Malate
Generic name (nonproprietary)
sunitinib malate
Active ingredients
Sunitinib malate — 50 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Teva Pharmaceuticals USA, Inc.NDC labeler code 0093
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213803
Marketing start
Listing expires
Other FDA classes
Protein Kinase Inhibitors (Mechanism)
Identifiers
Product ID 0093-8231_71bcc3b2-9dea-4700-af34-a9a5d2b708a2SPL ID 71bcc3b2-9dea-4700-af34-a9a5d2b708a2SPL set ID a9479e5f-914f-46ca-95c1-327c66457e47RxCUI 616279, 616285, 616289, 1541890UNII LVX8N1UT73
Pharmacologic class
Kinase Inhibitor

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

N400093823128 followed by a unit qualifier and the quantity

Package 00093-8231-28. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Sunitinib malate capsules are a kinase inhibitor indicated for: treatment of adult patients with gastrointestinal stromal tumor (GIST) after disease progression on or intolerance to imatinib mesylate. ( 1.1 ) treatment of adult patients with advanced renal cell carcinoma (RCC). ( 1.2 ) adjuvant treatment of adult patients at high risk of recurrent RCC following nephrectomy. ( 1.3 ) treatment of progressive, well-differentiated pancreatic neuroendocrine tumors (pNET) in adult patients with unresectable locally advanced or metastatic disease. ( 1.4) 1.1 Gastrointestinal Stromal Tumor Sunitinib malate capsules are indicated for the treatment of adult patients with gastrointestinal stromal tumor…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0093-8231

What is NDC 0093-8231?
0093-8231 is the product NDC for Sunitinib Malate, Sunitinib malate 50 mg/1 capsule, listed with the FDA by Teva Pharmaceuticals USA, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sunitinib Malate.
What is the active ingredient?
Sunitinib malate.
Who is the labeler?
Teva Pharmaceuticals USA, Inc., NDC labeler code 0093. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sunitinib Malate?
31 other product NDCs are listed under this name. See all Sunitinib Malate 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 Sunitinib Malate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Sunitinib MalateSunitinib malate 12.5 mg/1CapsuleOralNovadoz Pharmaceuticals LLC72205-11672205-0116-28
Sunitinib MalateSunitinib malate 25 mg/1CapsuleOralNovadoz Pharmaceuticals LLC72205-11772205-0117-28
Sunitinib MalateSunitinib malate 37.5 mg/1CapsuleOralNovadoz Pharmaceuticals LLC72205-11872205-0118-28
Sunitinib MalateSunitinib malate 50 mg/1CapsuleOralNovadoz Pharmaceuticals LLC72205-11972205-0119-28
Sunitinib MalateSunitinib malate 12.5 mg/1CapsuleOralNovugen Pharma (USA) LLC.82293-01482293-0014-10
Sunitinib MalateSunitinib malate 25 mg/1CapsuleOralNovugen Pharma (USA) LLC.82293-01582293-0015-10
Sunitinib MalateSunitinib malate 37.5 mg/1CapsuleOralNovugen Pharma (USA) LLC.82293-01682293-0016-10
Sunitinib MalateSunitinib malate 50 mg/1CapsuleOralNovugen Pharma (USA) LLC.82293-01782293-0017-10
Sunitinib MalateSunitinib malate 12.5 mg/1CapsuleOralAurobindo Pharma Limited59651-46459651-0464-2859651-0464-29
Sunitinib MalateSunitinib malate 25 mg/1CapsuleOralAurobindo Pharma Limited59651-46559651-0465-2859651-0465-29

All 32 Sunitinib Malate NDCs

Other NDCs under ANDA 213803

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

FDA NDC Directory listings under ANDA 213803
ProductStrengthForm · routeLabelerProduct NDC
Sunitinib MalateSunitinib malate 12.5 mg/1CapsuleOralTeva Pharmaceuticals USA, Inc.0093-8199
Sunitinib MalateSunitinib malate 25 mg/1CapsuleOralTeva Pharmaceuticals USA, Inc.0093-8224
Sunitinib MalateSunitinib malate 37.5 mg/1CapsuleOralTeva Pharmaceuticals USA, Inc.0093-8229
Sunitinib MalateSunitinib malate 12.5 mg/1CapsuleOralAvKARE42291-901
Sunitinib MalateSunitinib malate 25 mg/1CapsuleOralAvKARE42291-902
Sunitinib MalateSunitinib malate 37.5 mg/1CapsuleOralAvKARE42291-903
Sunitinib MalateSunitinib malate 50 mg/1CapsuleOralAvKARE42291-904

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