NDC codes

FDA NDC Directory
Product NDC (as listed)70377-083Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70377-0083Add 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
70377-083-117037700831160 TABLET, FILM COATED in 1 BOTTLE (70377-083-11)Marketed from Mar 3, 2025

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)
Dasatinib
Generic name (nonproprietary)
dasatinib
Active ingredients
Dasatinib20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217217
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 3A4 Inhibitors (Mechanism)Protein Kinase Inhibitors (Mechanism)
Identifiers
Product ID 70377-083_6718ab7c-7205-4927-4055-0ce76dfca7acSPL ID 6718ab7c-7205-4927-4055-0ce76dfca7acSPL set ID 76e1833c-e105-5a3d-0f01-1330d8cc7ae1RxCUI 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

N470377008311 followed by a unit qualifier and the quantity

Package 70377-0083-11. 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)

Other NDCs under ANDA 217217

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

FDA NDC Directory listings under ANDA 217217
ProductStrengthForm · routeLabelerProduct NDC
DasatinibDasatinib 70 mg/1Tablet, Film coatedOralBiocon Pharma Inc.70377-085
DasatinibDasatinib 50 mg/1Tablet, Film coatedOralBiocon Pharma Inc.70377-084
DasatinibDasatinib 80 mg/1Tablet, Film coatedOralBiocon Pharma Inc.70377-086
DasatinibDasatinib 100 mg/1Tablet, Film coatedOralBiocon Pharma Inc.70377-087
DasatinibDasatinib 140 mg/1Tablet, Film coatedOralBiocon Pharma Inc.70377-088
DasatinibDasatinib 50 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-661
DasatinibDasatinib 20 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-660
DasatinibDasatinib 100 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-664
DasatinibDasatinib 70 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-662
DasatinibDasatinib 80 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-663
DasatinibDasatinib 140 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-665

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