Norepinephrine Bitartrate Injection, Solution, Concentrate
NDC Package 0781-3755-95
Package Information
Norepinephrine Bitartrate injection is for blood pressure control in certain acute hypotensive states (e.g., pheochromocytomectomy, sympathectomy, poliomyelitis, spinal anesthesia, myocardial infarction, septicemia, blood transfusion, and drug reactions).As an adjunct in the treatment of cardiac arrest and profound hypotension. This formulation utilizes a injection, solution, concentrate delivery system. Marketed by Sandoz Inc, this product is identified by NDC 0781-3755 and is authorized under FDA application ANDA211359.
Identification & Billing
- RxCUI: 242969 - norepinephrine bitartrate 4 MG in 4 mL Injection
- RxCUI: 242969 - 4 ML norepinephrine 1 MG/ML Injection
- RxCUI: 242969 - norepinephrine (as bitartrate) 4 MG per 4 ML Injection
- RxCUI: 242969 - norepinephrine 4 MG per 4 ML Injection
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0781 - Sandoz Inc
- 0781-3755 - Norepinephrine Bitartrate
- 0781-3755-95 - 10 VIAL, SINGLE-DOSE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-DOSE (0781-3755-75)
- 0781-3755 - Norepinephrine Bitartrate
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 0781-3755-95 identifies a specific commercial package of 10 vial, single-dose in 1 carton / 4 ml in 1 vial, single-dose (0781-3755-75) of Norepinephrine Bitartrate, a human prescription drug labeled by Sandoz Inc. This injection, solution, concentrate is formulated for intravenous use and contains norepinephrine bitartrate 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 Sandoz Inc on April 23, 2019. The current certification is valid through December 31, 2026.
How is this Sandoz Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00781375595. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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 Labeler segment to maintain the 5-4-2 structure.