Somavert Kit
NDC Package 0009-7166-01
Package Information
Somavert (pegvisomant) kits is pegvisomant is used to treat a certain condition called acromegaly. This formulation utilizes a kit delivery system. Marketed by Pharmacia & Upjohn Company Llc, this product is identified by NDC 0009-7166 and is authorized under FDA application BLA021106.
Identification & Billing
- RxCUI: 1549323 - pegvisomant 25 MG Injection
- RxCUI: 1549452 - pegvisomant 30 MG Injection
- RxCUI: 1549454 - Somavert 30 MG Injection
- RxCUI: 1549454 - pegvisomant 30 MG Injection [Somavert]
- RxCUI: 1549456 - Somavert 25 MG Injection
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0009 - Pharmacia & Upjohn Company Llc
- 0009-7166 - Somavert
- 0009-7166-01 - 1 KIT in 1 CARTON * 1 mL in 1 VIAL, SINGLE-DOSE (0009-5175-02) * 1 mL in 1 SYRINGE (0009-5936-01)
- 0009-7166 - Somavert
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 (0009-7166). 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 0009-7166-01 identifies a specific commercial package of 1 kit in 1 carton * 1 ml in 1 vial, single-dose (0009-5175-02) * 1 ml in 1 syringe (0009-5936-01) of Somavert, a human prescription drug labeled by Pharmacia & Upjohn Company Llc. This kit is formulated for use and contains 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 Pharmacia & Upjohn Company Llc on October 01, 2016. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
Pegvisomant is used to treat a certain condition called acromegaly. Acromegaly occurs when the body makes too much growth hormone and other natural substances such as insulin-like growth factor-I (IGF-I). Pegvisomant is usually used if you have not responded to other treatments (such as surgery, radiation, other medications). Treating acromegaly helps reduce the risk of serious problems such as diabetes and heart disease. Pegvisomant works by blocking the action of growth hormone and by reducing the amount of IGF-I to normal levels.
How is this Pharmacia & Upjohn Company Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00009716601. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. 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.