NDC codes

FDA NDC Directory
Product NDC (as listed)70748-104Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70748-0104Add 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
70748-104-06707480104067074801040630 TABLET, EXTENDED RELEASE in 1 BOTTLE (70748-104-06)Marketed from Apr 17, 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

Generic name (nonproprietary)
dapagliflozin and metformin hydrochloride
Active ingredients
Dapagliflozin — 10 mg/1Metformin hydrochloride — 1000 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Lupin Pharmaceuticals, Inc.NDC labeler code 70748
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211579
Marketing start
Listing expires
Other FDA classes
Biguanides (Chemical structure)Sodium-Glucose Transporter 2 Inhibitors (Mechanism)
Identifiers
Product ID 70748-104_deac53e9-671e-4972-b0fa-9fdf2652a682SPL ID deac53e9-671e-4972-b0fa-9fdf2652a682

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

N470748010406 followed by a unit qualifier and the quantity

Package 70748-0104-06. 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

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

About NDC 70748-104

What is NDC 70748-104?
70748-104 is the product NDC for Dapagliflozin And Metformin Hydrochloride, Dapagliflozin 10 mg/1; Metformin hydrochloride 1000 mg/1 tablet, extended release, 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?
Dapagliflozin And Metformin Hydrochloride.
What is the active ingredient?
Dapagliflozin, Metformin hydrochloride.
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 Dapagliflozin And Metformin Hydrochloride?
31 other product NDCs are listed under this name. See all Dapagliflozin And Metformin Hydrochloride 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 Dapagliflozin And Metformin Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Dapagliflozin and Metformin HydrochlorideDapagliflozin 10 mg/1; Metformin hydrochloride 1000 mg/1Tablet, Film coated, Extended releaseOralMicro Labs Limited42571-32342571-0323-0442571-0323-3042571-0323-90
Dapagliflozin and Metformin HydrochlorideDapagliflozin 5 mg/1; Metformin hydrochloride 500 mg/1Tablet, Film coated, Extended releaseOralMicro Labs Limited42571-32042571-0320-0542571-0320-3042571-0320-90
Dapagliflozin and Metformin HydrochlorideDapagliflozin 10 mg/1; Metformin hydrochloride 500 mg/1Tablet, Film coated, Extended releaseOralMicro Labs Limited42571-32142571-0321-0542571-0321-3042571-0321-90
Dapagliflozin and Metformin HydrochlorideDapagliflozin 5 mg/1; Metformin hydrochloride 1000 mg/1Tablet, Film coated, Extended releaseOralMicro Labs Limited42571-32242571-0322-3042571-0322-6042571-0322-90
Dapagliflozin And Metformin HydrochlorideDapagliflozin 5 mg/1; Metformin hydrochloride 500 mg/1Tablet, Extended releaseOralLupin Pharmaceuticals, Inc.70748-10170748-0101-06
Dapagliflozin And Metformin HydrochlorideDapagliflozin 5 mg/1; Metformin hydrochloride 1000 mg/1Tablet, Extended releaseOralLupin Pharmaceuticals, Inc.70748-10270748-0102-07
Dapagliflozin And Metformin HydrochlorideDapagliflozin 10 mg/1; Metformin hydrochloride 500 mg/1Tablet, Extended releaseOralLupin Pharmaceuticals, Inc.70748-10370748-0103-06
Dapagliflozin and Metformin HydrochlorideDapagliflozin 10 mg/1; Metformin hydrochloride 500 mg/1Tablet, Extended releaseOralMacleods Pharmaceuticals Limited33342-40733342-0407-0633342-0407-0733342-0407-09+2 more
Dapagliflozin and Metformin HydrochlorideDapagliflozin 5 mg/1; Metformin hydrochloride 1000 mg/1Tablet, Extended releaseOralMacleods Pharmaceuticals Limited33342-40833342-0408-0633342-0408-0733342-0408-09+2 more
Dapagliflozin and Metformin HydrochlorideDapagliflozin 10 mg/1; Metformin hydrochloride 1000 mg/1Tablet, Extended releaseOralMacleods Pharmaceuticals Limited33342-40933342-0409-0633342-0409-0733342-0409-09+2 more

All 32 Dapagliflozin And Metformin Hydrochloride NDCs

Other NDCs under ANDA 211579

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

FDA NDC Directory listings under ANDA 211579
ProductStrengthForm · routeLabelerProduct NDC
Dapagliflozin And Metformin HydrochlorideDapagliflozin 5 mg/1; Metformin hydrochloride 500 mg/1Tablet, Extended releaseOralLupin Pharmaceuticals, Inc.70748-101
Dapagliflozin And Metformin HydrochlorideDapagliflozin 5 mg/1; Metformin hydrochloride 1000 mg/1Tablet, Extended releaseOralLupin Pharmaceuticals, Inc.70748-102
Dapagliflozin And Metformin HydrochlorideDapagliflozin 10 mg/1; Metformin hydrochloride 500 mg/1Tablet, Extended releaseOralLupin Pharmaceuticals, Inc.70748-103

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