Furosemide Injection, Solution
NDC Package 70756-620-10
Package Information
Furosemide injection is parenteral therapy should be reserved for patients unable to take oral medication or for patients in emergency clinical situations.Edema: Furosemide is indicated in adults and pediatric patients for the treatment of edema associated with congestive heart failure, cirrhosis of the liver, and renal disease, including the nephrotic syndrome. This formulation utilizes a injection, solution delivery system. Marketed by Lifestar Pharma Llc, this product is identified by NDC 70756-620 and is authorized under FDA application ANDA216860.
Identification & Billing
- RxCUI: 1719286 - furosemide 100 MG in 10 ML Injection
- RxCUI: 1719286 - 10 ML furosemide 10 MG/ML Injection
- RxCUI: 1719286 - furosemide 100 MG per 10 ML Injection
- RxCUI: 1719290 - furosemide 20 MG in 2 ML Injection
- RxCUI: 1719290 - 2 ML furosemide 10 MG/ML Injection
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 70756 - Lifestar Pharma Llc
- 70756-620 - Furosemide
- 70756-620-10 - 10 VIAL in 1 CARTON / 10 mL in 1 VIAL (70756-620-86)
- 70756-620 - Furosemide
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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Other Available Packages
The following commercial packages are registered under the same Product NDC (70756-620). 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 70756-620-10 identifies a specific commercial package of 10 vial in 1 carton / 10 ml in 1 vial (70756-620-86) of Furosemide, a human prescription drug labeled by Lifestar Pharma Llc. This injection, solution is formulated for intravenous use and contains furosemide 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 Lifestar Pharma Llc on December 17, 2022. The current certification is valid through December 31, 2027.
How is this Lifestar Pharma Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 70756062010. 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.