Kit For The Prepartion Of Technetium Tc99m Sulfur Colloid Kit
NDC Package 45567-0030-1
Package Information
Kit For The Prepartion Of Technetium Tc99m Sulfur Colloid (technetium tc 99m sulfur colloid) kits is technetium Tc 99m Sulfur Colloid Injection is indicated:In adults, to assist in the: •localization of lymph nodes draining a primary tumor in patients with breast cancer or malignant melanoma when used with a hand-held gamma counter.•evaluation of peritoneo-venous (LeVeen) shunt patency.In adults and pediatric patients, for imaging:•areas of functioning reticuloendothelial cells in the liver, spleen and bone marrow.•studies of esophageal transit and, gastroesophageal reflux, and detection of pulmonary aspiration of gastric contents. This formulation utilizes a kit delivery system. Marketed by Sun Pharmaceutical Industries, Inc., this product is identified by NDC 45567-0030 and is authorized under FDA application NDA017858.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 45567 - Sun Pharmaceutical Industries, Inc.
- 45567-0030 - Kit For The Prepartion Of Technetium Tc99m Sulfur Colloid
- 45567-0030-1 - 1 KIT in 1 PACKAGE * 3 mL in 1 VIAL * 3 mL in 1 VIAL * 10 mL in 1 VIAL
- 45567-0030 - Kit For The Prepartion Of Technetium Tc99m Sulfur Colloid
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 45567-0030-1 identifies a specific commercial package of 1 kit in 1 package * 3 ml in 1 vial * 3 ml in 1 vial * 10 ml in 1 vial of Kit For The Prepartion Of Technetium Tc99m Sulfur Colloid, a human prescription drug labeled by Sun Pharmaceutical Industries, Inc.. 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 Sun Pharmaceutical Industries, Inc. on April 19, 1978. The current certification is valid through December 31, 2026.
How is this Sun Pharmaceutical Industries, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 45567003001. 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 Package segment to maintain the 5-4-2 structure.