NDC codes

FDA NDC Directory
Product NDC (as listed)27241-151Labeler and product segments. Claims need a package NDC.
Product NDC at billing width27241-0151Add 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
27241-151-012724101510130 TABLET in 1 BOTTLE (27241-151-01)Marketed from Apr 6, 2026
27241-151-902724101519090 TABLET in 1 BOTTLE (27241-151-90)Marketed from Sep 2, 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)
Dapagliflozin
Generic name (nonproprietary)
dapagliflozin
Active ingredients
Dapagliflozin5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211482
Marketing start
Listing expires
Other FDA classes
Sodium-Glucose Transporter 2 Inhibitors (Mechanism)
Identifiers
Product ID 27241-151_af7c3e48-a7c2-4f5a-b812-b0c089fa2a79SPL ID af7c3e48-a7c2-4f5a-b812-b0c089fa2a79

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

N427241015101 followed by a unit qualifier and the quantity

Package 27241-0151-01. 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 211482

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

FDA NDC Directory listings under ANDA 211482
ProductStrengthForm · routeLabelerProduct NDC
DapagliflozinDapagliflozin 10 mg/1TabletOralAjanta Pharma USA Inc.27241-152

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