NDC codes

FDA NDC Directory
Product NDC (as listed)72205-321Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72205-0321Add 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
72205-321-607220503216060 TABLET in 1 BOTTLE (72205-321-60)Marketed from Sep 11, 2026

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
Dasatinib — 70 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 219579
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 3A4 Inhibitors (Mechanism)Protein Kinase Inhibitors (Mechanism)
Identifiers
Product ID 72205-321_bffb38c3-f556-492f-a9db-aa417ec0a856SPL ID bffb38c3-f556-492f-a9db-aa417ec0a856
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

N472205032160 followed by a unit qualifier and the quantity

Package 72205-0321-60. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 219579

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

FDA NDC Directory listings under ANDA 219579
ProductStrengthForm · routeLabelerProduct NDC
DasatinibDasatinib 20 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-319
DasatinibDasatinib 50 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-320
DasatinibDasatinib 80 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-322
DasatinibDasatinib 100 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-323
DasatinibDasatinib 140 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-324

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