NDC codes

FDA NDC Directory
Product NDC (as listed)0480-5101Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00480-5101Add 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
0480-5101-06004805101060048051010660 TABLET, FILM COATED in 1 BOTTLE (0480-5101-06)Marketed from Sep 18, 2025

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)
Dasatinib
Generic name (nonproprietary)
dasatinib
Active ingredients
Dasatinib — 20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Teva Pharmaceuticals, Inc.NDC labeler code 0480
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211094
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 3A4 Inhibitors (Mechanism)Protein Kinase Inhibitors (Mechanism)
Identifiers
Product ID 0480-5101_97769ebd-872d-4851-bf3f-51630e995dd6SPL ID 97769ebd-872d-4851-bf3f-51630e995dd6SPL set ID 3000fd91-1b09-4d72-8522-1ca5e35ed956RxCUI 643105, 643107, 643109, 799047, 1045402, 1045406UNII RBZ1571X5H
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

N400480510106 followed by a unit qualifier and the quantity

Package 00480-5101-06. 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 .

Indications (excerpt from the label)

Dasatinib tablets are indicated for the treatment of adult patients with newly diagnosed Philadelphia chromosome-positive (Ph+) chronic myeloid leukemia (CML) in chronic phase. chronic, accelerated, or myeloid or lymphoid blast phase Ph+ CML with resistance or intolerance to prior therapy including imatinib. Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) with resistance or intolerance to prior therapy. Dasatinib tablets are indicated for the treatment of pediatric patients 1 year of age and older with Ph+ CML in chronic phase. newly diagnosed Ph+ ALL in combination with chemotherapy. Dasatinib tablets are a kinase inhibitor indicated for the treatment of newly diagno…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0480-5101

What is NDC 0480-5101?
0480-5101 is the product NDC for Dasatinib, Dasatinib 20 mg/1 tablet, film coated, listed with the FDA by Teva Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Dasatinib.
What is the active ingredient?
Dasatinib.
Who is the labeler?
Teva Pharmaceuticals, Inc., NDC labeler code 0480. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dasatinib?
95 other product NDCs are listed under this name. See all Dasatinib 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 Dasatinib NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
DasatinibDasatinib 20 mg/1Tablet, Film coatedOralQuallent Pharmaceuticals Health LLC82009-19282009-0192-60
DasatinibDasatinib 100 mg/1Tablet, Film coatedOralQuallent Pharmaceuticals Health LLC82009-19682009-0196-30
DasatinibDasatinib 50 mg/1Tablet, Film coatedOralQuallent Pharmaceuticals Health LLC82009-19382009-0193-60
DasatinibDasatinib 70 mg/1Tablet, Film coatedOralQuallent Pharmaceuticals Health LLC82009-19482009-0194-60
DasatinibDasatinib 80 mg/1Tablet, Film coatedOralQuallent Pharmaceuticals Health LLC82009-19582009-0195-30
DasatinibDasatinib 140 mg/1Tablet, Film coatedOralQuallent Pharmaceuticals Health LLC82009-19782009-0197-30
DasatinibDasatinib 20 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-31972205-0319-60
DasatinibDasatinib 100 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-32372205-0323-30
DasatinibDasatinib 50 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-32072205-0320-60
DasatinibDasatinib 70 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-32172205-0321-60

All 96 Dasatinib NDCs

Other NDCs under ANDA 211094

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

FDA NDC Directory listings under ANDA 211094
ProductStrengthForm · routeLabelerProduct NDC
DasatinibDasatinib 80 mg/1Tablet, Film coatedOralTeva Pharmaceuticals, Inc.0480-3523
DasatinibDasatinib 140 mg/1Tablet, Film coatedOralTeva Pharmaceuticals, Inc.0480-3524
DasatinibDasatinib 50 mg/1Tablet, Film coatedOralTeva Pharmaceuticals, Inc.0480-5102
DasatinibDasatinib 70 mg/1Tablet, Film coatedOralTeva Pharmaceuticals, Inc.0480-5103
DasatinibDasatinib 100 mg/1Tablet, Film coatedOralTeva Pharmaceuticals, Inc.0480-5104
DasatinibDasatinib 20 mg/1Tablet, Film coatedOralAvKARE73190-046
DasatinibDasatinib 50 mg/1Tablet, Film coatedOralAvKARE73190-047
DasatinibDasatinib 70 mg/1Tablet, Film coatedOralAvKARE73190-048
DasatinibDasatinib 80 mg/1Tablet, Film coatedOralAvKARE73190-049
DasatinibDasatinib 100 mg/1Tablet, Film coatedOralAvKARE73190-050
DasatinibDasatinib 140 mg/1Tablet, Film coatedOralAvKARE73190-051

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