Dapagliflozin Tablet
NDC Package 71921-421-33

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Dapagliflozin tablets are indicated:  To reduce the risk of hospitalization for heart failure in adults with type 2 diabetes mellitus and either established cardiovascular disease or multiple cardiovascular risk factors.  As an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.Limitations  of UseDapagliflozin tablets are not recommended for use to improve glycemic control in patients with type 1 diabetes mellitus [see Warnings and Precautions (5.1)]. This formulation utilizes a tablet delivery system. Marketed by Florida Pharmaceutical Products, Llc, this product is identified by NDC 71921-421 and is authorized under FDA application ANDA211156.

Identification & Billing

NDC Package Code
71921-421-33
Package Description
30 TABLET in 1 BOTTLE
Product Code
71921-421
11-Digit Billing Format
71921042133
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
30 EA
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Dapagliflozin
Non-Proprietary Name
Dapagliflozin
Substance Name
Dapagliflozin
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
DAPAGLIFLOZIN 10 mg/1
Pharmacologic Class
Usage Information
Dapagliflozin tablets are indicated:  To reduce the risk of hospitalization for heart failure in adults with type 2 diabetes mellitus and either established cardiovascular disease or multiple cardiovascular risk factors.  As an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.Limitations  of UseDapagliflozin tablets are not recommended for use to improve glycemic control in patients with type 1 diabetes mellitus [see Warnings and Precautions (5.1)]. Dapagliflozin tablets are 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 tablets are likely to be ineffective in this setting based upon its mechanism of action. Pediatric use information is approved for AstraZeneca AB's Farxiga ®(dapagliflozin) Tablets. However, due to AstraZeneca AB's marketing exclusivity rights, this drug product is not labeled with that information.

Regulatory & Marketing

Labeler Name
Florida Pharmaceutical Products, Llc
Product Type
Human Prescription Drug
FDA Application #
ANDA211156
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
04-06-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (71921-421). Click a package code to view its specific billing and regulatory data.

71921-421-09
90 TABLET in 1 BOTTLE
71921-421-50
500 TABLET in 1 BOTTLE

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 71921-421-33 identifies a specific commercial package of 30 tablet in 1 bottle of Dapagliflozin, a human prescription drug labeled by Florida Pharmaceutical Products, Llc. This tablet is formulated for oral use and contains dapagliflozin as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Florida Pharmaceutical Products, Llc on April 06, 2026. The current certification is valid through December 31, 2027.

How is this Florida Pharmaceutical Products, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71921042133. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 30 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
71921-421-33
11-Digit CMS (5-4-2)
71921-0421-33

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.