NDC codes

FDA NDC Directory
Product NDC (as listed)63304-092Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63304-0092Add 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
63304-092-276330400922728 CAPSULE in 1 BOTTLE (63304-092-27)Marketed from Dec 25, 2019
63304-092-86633040092864 BLISTER PACK in 1 BOX (63304-092-86) / 7 CAPSULE in 1 BLISTER PACK (63304-092-11)Marketed from Dec 25, 2019

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)
Sunitinib malate
Generic name (nonproprietary)
sunitinib malate
Active ingredients
Sunitinib malate — 25 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213914
Marketing start
Listing expires
Other FDA classes
Protein Kinase Inhibitors (Mechanism)
Identifiers
Product ID 63304-092_2971c7ca-50dc-e36c-e063-6294a90a4b7dSPL ID 2971c7ca-50dc-e36c-e063-6294a90a4b7dSPL set ID 06e0ad28-6637-4f54-879c-2c194aece5fdRxCUI 616279, 616285, 616289, 1541890UNII LVX8N1UT73UPC 0363304092271
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

N463304009227 followed by a unit qualifier and the quantity

Package 63304-0092-27. 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 (GIST)…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 213914

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

FDA NDC Directory listings under ANDA 213914
ProductStrengthForm · routeLabelerProduct NDC
Sunitinib malateSunitinib malate 12.5 mg/1CapsuleOralSun Pharmaceutical Industries Inc.63304-091
Sunitinib malateSunitinib malate 37.5 mg/1CapsuleOralSun Pharmaceutical Industries Inc.63304-093
Sunitinib malateSunitinib malate 50 mg/1CapsuleOralSun Pharmaceutical Industries Inc.63304-094
Sunitinib malateSunitinib malate 12.5 mg/1CapsuleOralNorthStar RxLLC16714-676
Sunitinib malateSunitinib malate 25 mg/1CapsuleOralNorthStar RxLLC16714-677
Sunitinib malateSunitinib malate 37.5 mg/1CapsuleOralNorthStar RxLLC16714-678
Sunitinib malateSunitinib malate 50 mg/1CapsuleOralNorthStar RxLLC16714-679

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