Thiamine Hydrochloride Injection, Solution
NDC Package 72603-565-25
Package Information
Thiamine Hydrochloride injection is effective for the treatment of thiamine deficiency or beriberi whether of the dry (major symptoms related to the nervous system) or wet (major symptoms related to the cardiovascular system) variety. Thiamine hydrochloride injection should be used where rapid restoration of thiamine is necessary, as in Wernicke’s encephalopathy, infantile beriberi with acute collapse, cardiovascular disease due to thiamine deficiency, or neuritis of pregnancy if vomiting is severe. It is also indicated when giving IV dextrose to individuals with marginal thiamine status to avoid precipitation of heart failure.Thiamine hydrochloride injection is also indicated in patients with established thiamine deficiency who cannot take thiamine orally due to coexisting severe anorexia, nausea, vomiting, or malabsorption. Thiamine hydrochloride injection is not usually indicated for conditions of decreased oral intake or decreased gastrointestinal absorption, because multiple vitamins should usually be given. This formulation utilizes a injection, solution delivery system. Marketed by Northstar Rxllc, this product is identified by NDC 72603-565 and is authorized under FDA application ANDA218471.
Identification & Billing
Clinical Specifications
- Intramuscular - Administration within a muscle.
- Intravenous - Administration within or into a vein or veins.
Regulatory & Marketing
Hierarchy Structure
- 72603 - Northstar Rxllc
- 72603-565 - Thiamine Hydrochloride
- 72603-565-25 - 25 VIAL, MULTI-DOSE in 1 CARTON / 2 mL in 1 VIAL, MULTI-DOSE (72603-565-01)
- 72603-565 - Thiamine Hydrochloride
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 72603-565-25 identifies a specific commercial package of 25 vial, multi-dose in 1 carton / 2 ml in 1 vial, multi-dose (72603-565-01) of Thiamine Hydrochloride, a human prescription drug labeled by Northstar Rxllc. This injection, solution is formulated for intramuscular; intravenous use and contains thiamine hydrochloride 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 Northstar Rxllc on October 14, 2026. The current certification is valid through December 31, 2027.
How is this Northstar Rxllc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 72603056525. 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.