Sitagliptin And Metformin Hydrochloride Tablet, Film Coated
NDC Package 70710-1986-8
Package Information
Sitagliptin And Metformin Hydrochloride tablets is classified as a
administered via oral route. This formulation utilizes a tablet, film coated delivery system. Marketed by Zydus Pharmaceuticals (usa) Inc., this product is identified by NDC 70710-1986 and is authorized under FDA application NDA216743.Identification & Billing
- RxCUI: 861769 - SITagliptin 50 MG / metFORMIN HCl 1000 MG Oral Tablet
- RxCUI: 861769 - metformin hydrochloride 1000 MG / sitagliptin 50 MG Oral Tablet
- RxCUI: 861819 - SITagliptin 50 MG / metFORMIN HCl 500 MG Oral Tablet
- RxCUI: 861819 - metformin hydrochloride 500 MG / sitagliptin 50 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 70710 - Zydus Pharmaceuticals (usa) Inc.
- 70710-1986 - Sitagliptin And Metformin Hydrochloride
- 70710-1986-8 - 180 TABLET, FILM COATED in 1 BOTTLE
- 70710-1986 - Sitagliptin And Metformin Hydrochloride
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 (70710-1986). Click a package code to view its specific billing and regulatory data.
* 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 70710-1986-8 identifies a specific commercial package of 180 tablet, film coated in 1 bottle of Sitagliptin And Metformin Hydrochloride, a human prescription drug labeled by Zydus Pharmaceuticals (usa) Inc.. This tablet, film coated is formulated for oral use and contains metformin hydrochloride; sitagliptin 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 Zydus Pharmaceuticals (usa) Inc. on March 14, 2024. The current certification is valid through December 31, 2026.
How is this Zydus Pharmaceuticals (usa) Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 70710198608. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.