Dapagliflozin NDC 70710-1380

NDC codes

FDA NDC Directory

Product NDC (as listed)70710-1380Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70710-1380Add 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 NDC	11-digit (billing)	Package	Copy
70710-1380-3	70710138003	30 TABLET in 1 BOTTLE (70710-1380-3)Marketed from Apr 6, 2026
70710-1380-9	70710138009	90 TABLET in 1 BOTTLE (70710-1380-9)Marketed from Apr 6, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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: Dapagliflozin — 5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Zydus Pharmaceuticals USA Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211582
Marketing start: Apr 6, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Sodium-Glucose Transporter 2 Inhibitors (Mechanism)
Identifiers: Product ID 70710-1380_3701f266-4f18-4271-a3d6-447fe86ff6cbSPL ID 3701f266-4f18-4271-a3d6-447fe86ff6cbSPL set ID 17586ec6-0104-4b08-ad87-12a837568d6cRxCUI 1488569, 1488574UNII 1ULL0QJ8UCUPC 0370710138134, 0370710138035
Pharmacologic class: Sodium-Glucose Cotransporter 2 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

N470710138003 followed by a unit qualifier and the quantity

Package 70710-1380-03. 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 Jun 22, 2026.

Indications (excerpt from the label)

Dapagliflozin tablets are indicated: To reduce the risk of hospitalization for heart failure in adults with type 2 diabetes mellitus and either established CV disease or multiple CV risk factors. As an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. Limitations of Use Dapagliflozin tablets are not recommended for use to improve glycemic control in patients with type 1 diabetes mellitus. [see Warnings and Precautions ( 5.1 )]. Dapagliflozin is not recommended for use to improve glycemic control in patients with type 2 diabetes mellitus with an eGFR less than 45 mL/min/1.73 m 2 . Dapagliflozin is likely to be ineffective in this setting based u…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 211582

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

FDA NDC Directory listings under ANDA 211582
Product	Strength	Form · route	Labeler	Product NDC
Dapagliflozin	Dapagliflozin 5 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1714
Dapagliflozin	Dapagliflozin 10 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1715
Dapagliflozin	Dapagliflozin 10 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	70710-1381