Baclofen (intrathecal) Injection
Product Images NDC 70511-124

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Baclofen (intrathecal) (NDC 70511-124). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Maia Pharmaceuticals, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Baclofen Structure (Baclofen 01)

FDA Label Image

Carton Label Ndc 70511-124-10 (Carton 2000mcg)

Carton Label Ndc 70511-124-10 (Carton 2000mcg)
This is a description of Baclofen Injection produced by MAIA Pharmaceuticals. It is a 40mg/20mL solution that is not required to be refrigerated or frozen, and should be stored between 20° to 25°C. The injection is for intrathecal use only and contains baclofen and sodium chloride. The medication details and prescription instructions are provided on the packaging. Lot and expiration information is also listed.*
FDA Label Image

Carton Ndc 70511-122-20 (Carton 500mcg)

Carton Ndc 70511-122-20 (Carton 500mcg)
This is a medication label for Baclofen Injection intended for intrathecal use. It contains 10mg/20mL of baclofen and is manufactured for M Pharmaceuticals. The drug should not be frozen or refrigerated and should be stored at room temperature. The dosage instructions are not available. The label includes a lot number and barcode.*
FDA Label Image

Container Label Ndc 70511-124-10 (Vial Label 2000mcg)

FDA Label Image

Vial Ndc 70511-122-20 (Vial Label 500mcg)

Vial Ndc 70511-122-20 (Vial Label 500mcg)
This is a description of a medication with the NDC code 70511-122.20. The medication is called Baclofen Injection and is administered through intrathecal injection. It comes in a 20 mL single-dose vial with a strength of 10 mg/20 mL and a total volume of 500 megimL. The solution is sterile and manufactured by MAIA Pharmaceuticals in Princeton, NJ, with some indication that it may also be made in India. The prescription is labeled for immediate use only, and any unused portion should be discarded.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.