Tev-tropin
NDC Package 57844-716-19
Package Information
Tev-tropin is a . Marketed by Teva, this product is identified by NDC 57844-716 and is authorized under FDA application NDA019774.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 57844 - Teva
- 57844-716 - Tev-tropin
- 57844-716-19 - 1 KIT in 1 CARTON * 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL * 1 mL in 1 VIAL
- 57844-716 - Tev-tropin
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 57844-716-19 identifies a specific commercial package of 1 kit in 1 carton * 1 injection, powder, for solution in 1 vial * 1 ml in 1 vial of Tev-tropin, labeled by Teva. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Teva on May 25, 1995. The current certification is valid through September 01, 2015.
How is this Teva product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 57844071619. 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 Product segment to maintain the 5-4-2 structure.