Javygtor Powder, For Solution
NDC Package 43598-162-30
Package Information
Javygtor (sapropterin dihydrochloride) powders is a medication used along with diet changes for long-term treatment of a certain inherited disorder (phenylketonuria-PKU). This formulation utilizes a powder, for solution delivery system. Marketed by Dr. Reddys Laboratories Inc, this product is identified by NDC 43598-162 and is authorized under FDA application ANDA215798.
Identification & Billing
- RxCUI: 1653217 - sapropterin dihydrochloride 500 MG Powder for Oral Solution
- RxCUI: 2621237 - JAVYGTOR 500 MG Powder for Oral Solution
- RxCUI: 2621237 - sapropterin dihydrochloride 500 MG Powder for Oral Solution [Javygtor]
- RxCUI: 2621237 - Javygtor 500 MG Powder for Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 43598 - Dr. Reddys Laboratories Inc
- 43598-162 - Javygtor
- 43598-162-30 - 30 PACKET in 1 CARTON / 1 POWDER, FOR SOLUTION in 1 PACKET (43598-162-11)
- 43598-162 - Javygtor
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 43598-162-30 identifies a specific commercial package of 30 packet in 1 carton / 1 powder, for solution in 1 packet (43598-162-11) of Javygtor, a human prescription drug labeled by Dr. Reddys Laboratories Inc. This product is billed for "EA" each discreet unit and contains an estimated amount of 30 billable units per package. This powder, for solution is formulated for oral use and contains sapropterin dihydrochloride 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 Dr. Reddys Laboratories Inc on November 16, 2022. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
This medication is used along with diet changes for long-term treatment of a certain inherited disorder (phenylketonuria-PKU). It helps remove a certain chemical (phenylalanine) from the body. Too much phenylalanine in the body can cause brain damage.
How is this Dr. Reddys Laboratories Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43598016230. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 30 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 Product segment to maintain the 5-4-2 structure.