Baqsimi Powder
NDC Package 0548-8352-02
Package Information
Baqsimi (glucagon) powders is a medication the same as your body's own glucagon, a natural substance that raises blood sugar by causing the body to release sugar stored in the liver. This formulation utilizes a powder delivery system. Marketed by Amphastar Pharmaceuticals, Inc., this product is identified by NDC 0548-8352 and is authorized under FDA application NDA210134.
Identification & Billing
- RxCUI: 2180666 - glucagon 3 MG Nasal Powder
- RxCUI: 2180671 - baqsimi 3 MG Nasal Powder
- RxCUI: 2180671 - glucagon 3 MG Nasal Powder [Baqsimi]
- RxCUI: 2180671 - Baqsimi 3 MG Nasal Powder
Clinical Specifications
- Antihypoglycemic Agent - [EPC] (Established Pharmacologic Class)
- Decreased GI Motility - [PE] (Physiologic Effect)
- Decreased GI Smooth Muscle Tone - [PE] (Physiologic Effect)
- Decreased Glycolysis - [PE] (Physiologic Effect)
- Gastrointestinal Motility Inhibitor - [EPC] (Established Pharmacologic Class)
- Increased Gluconeogenesis - [PE] (Physiologic Effect)
- Increased Glycogenolysis - [PE] (Physiologic Effect)
Regulatory & Marketing
Hierarchy Structure
- 0548 - Amphastar Pharmaceuticals, Inc.
- 0548-8352 - Baqsimi
- 0548-8352-02 - 2 TUBE in 1 CARTON / 1 BOTTLE, UNIT-DOSE in 1 TUBE / 1 POWDER in 1 BOTTLE, UNIT-DOSE
- 0548-8352 - Baqsimi
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.
* 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 0548-8352-02 identifies a specific commercial package of 2 tube in 1 carton / 1 bottle, unit-dose in 1 tube / 1 powder in 1 bottle, unit-dose of Baqsimi, a human prescription drug labeled by Amphastar Pharmaceuticals, Inc.. This powder is formulated for nasal use and contains glucagon 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 Amphastar Pharmaceuticals, Inc. on July 24, 2019. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
This medication is the same as your body's own glucagon, a natural substance that raises blood sugar by causing the body to release sugar stored in the liver. It is used to treat very low blood sugar (hypoglycemia) that may cause you to need help from others. Make sure a family member or caregiver knows where you keep this medication and how to use it before you need their help.
How is this Amphastar Pharmaceuticals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00548835202. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 2 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 Labeler segment to maintain the 5-4-2 structure.