NDC 58281-561 Lioresal
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58281 - Medtronic Neuromodulation
- 58281-561 - Lioresal
Product Packages
NDC Code 58281-561-02
Package Description: 2 AMPULE in 1 PACKAGE, COMBINATION / 5 mL in 1 AMPULE
Product Details
What is NDC 58281-561?
What are the uses for Lioresal?
Which are Lioresal UNII Codes?
The UNII codes for the active ingredients in this product are:
- BACLOFEN (UNII: H789N3FKE8)
- BACLOFEN (UNII: H789N3FKE8) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Lioresal?
- RxCUI: 1666613 - baclofen 40 MG in 20 ML (2,000 MCG/ML) Injection
- RxCUI: 1666613 - 20 ML baclofen 2 MG/ML Injection
- RxCUI: 1666613 - baclofen 40,000 MCG per 20 ML Injection
- RxCUI: 1666620 - LIORESAL INTRATHECAL 40 MG in 20 ML (2,000 MCG/ML) Injection
- RxCUI: 1666620 - 20 ML baclofen 2 MG/ML Injection [Lioresal]
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".