Sodium Monofluorophosphate Powder
NDC Package 73608-000-25
Package Information
Sodium Monofluorophosphate powders is a bulk ingredient utilized for pharmaceutical compounding or manufacturing. This formulation utilizes a powder delivery system. Marketed by Bk Giulini Gmbh, this product is identified by NDC 73608-000.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 73608 - Bk Giulini Gmbh
- 73608-000 -
- 73608-000-25 - 25 kg in 1 BAG
- 73608-000 -
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 73608-000-25 identifies a specific commercial package of 25 kg in 1 bag of Sodium Monofluorophosphate (UNFINISHED drug), a bulk ingredient labeled by Bk Giulini Gmbh. This powder is formulated for use and contains sodium monofluorophosphate 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 Bk Giulini Gmbh on April 25, 2020. The current certification is valid through December 31, 2026.
How is this Bk Giulini Gmbh product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 73608000025. 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.