Cefdinir Powder, For Suspension
NDC Package 0093-4136-73
Package Information
Cefdinir powders is cefdinir is used to treat a wide variety of bacterial infections. This formulation utilizes a powder, for suspension delivery system. Marketed by Teva Pharmaceuticals Usa, Inc., this product is identified by NDC 0093-4136 and is authorized under FDA application ANDA065332.
Identification & Billing
- RxCUI: 309054 - cefdinir 125 MG in 5 mL Oral Suspension
- RxCUI: 309054 - cefdinir 25 MG/ML Oral Suspension
- RxCUI: 309054 - cefdinir 125 MG per 5 ML Oral Suspension
- RxCUI: 476576 - cefdinir 250 MG in 5 mL Oral Suspension
- RxCUI: 476576 - cefdinir 50 MG/ML Oral Suspension
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0093 - Teva Pharmaceuticals Usa, Inc.
- 0093-4136 - Cefdinir
- 0093-4136-73 - 100 mL in 1 BOTTLE
- 0093-4136 - Cefdinir
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 (0093-4136). 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 0093-4136-73 identifies a specific commercial package of 100 ml in 1 bottle of Cefdinir, a human prescription drug labeled by Teva Pharmaceuticals Usa, Inc.. This powder, for suspension is formulated for oral use and contains cefdinir monohydrate 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 Teva Pharmaceuticals Usa, Inc. on May 08, 2007. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
Cefdinir is used to treat a wide variety of bacterial infections. This medication is known as a cephalosporin antibiotic. It works by stopping the growth of bacteria. This antibiotic treats only bacterial infections. It will not work for viral infections (such as common cold, flu). Using any antibiotic when it is not needed can cause it to not work for future infections.
How is this Teva Pharmaceuticals Usa, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00093413673. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 100 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:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.