NDC codes

FDA NDC Directory
Product NDC (as listed)70748-212Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70748-0212Add 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
70748-212-0670748021206707480212061 BOTTLE in 1 CARTON (70748-212-06) / 30 TABLET in 1 BOTTLEMarketed from Jan 30, 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 — 100 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Lupin Pharmaceuticals, Inc.NDC labeler code 70748
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214350
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 3A4 Inhibitors (Mechanism)Protein Kinase Inhibitors (Mechanism)
Identifiers
Product ID 70748-212_79f45560-3318-42e3-8be6-fac133dca745SPL ID 79f45560-3318-42e3-8be6-fac133dca745SPL set ID f60261dd-b8ea-4511-bed6-ad6d7f4dd828RxCUI 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

N470748021206 followed by a unit qualifier and the quantity

Package 70748-0212-06. 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 kinase inhibitor indicated for the treatment of newly diagnose…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70748-212

What is NDC 70748-212?
70748-212 is the product NDC for Dasatinib, Dasatinib 100 mg/1 tablet, listed with the FDA by Lupin 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?
Lupin Pharmaceuticals, Inc., NDC labeler code 70748. 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 214350

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

FDA NDC Directory listings under ANDA 214350
ProductStrengthForm · routeLabelerProduct NDC
DasatinibDasatinib 20 mg/1TabletOralLupin Pharmaceuticals, Inc.70748-208
DasatinibDasatinib 50 mg/1TabletOralLupin Pharmaceuticals, Inc.70748-209
DasatinibDasatinib 70 mg/1TabletOralLupin Pharmaceuticals, Inc.70748-210
DasatinibDasatinib 80 mg/1TabletOralLupin Pharmaceuticals, Inc.70748-211
DasatinibDasatinib 140 mg/1TabletOralLupin Pharmaceuticals, Inc.70748-213

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