Product Images Hydralazine Hydrochloride

This is a description of the medication "Hydralazine Hydrochloride Injection, USP" provided in a 4 mL single-dose vial by the company NDGT2672265-01 RaOrly in Lehi, Utah. The warning mentions that any unused portion of the medication should be discarded. It should be stored within a USP Controlled Room temperature range of 20-25°C (66-77°F) and the package insert should be consulted for directions on use.*

hydrALAZINE Hydrochlorit Injection, USP is a sterile, nonpyrogenic solution for intramuscular or intravenous use only in emergency cases when the patient is unable to take oral medication. Each mL contains Hycralazine Hydrochloride 20 g, Propylene Glycol 036 mg, Methylparaben 065 mo, Popylaraben 0.35 g, and Water for Infection 5. The pH of the solution is 3.4-4.4 and can be adjusted using HycrocHlori Acid andio Sotum Hydroxde. The unused portion must be discarded. The storage temperature should be between 20°25°C (68"77°F). For directions on how to use this product, please refer to the Package Insert. There are 25 single-dose vials, each containing 1 mL of the solution, manufactured by American Regart located at Shitey New York 11667.*

This appears to be a product testing label that includes a lot number (not provided), expiration date of November 2020, and product identification numbers including a GTIN (Global Trade Item Number) and a serial number. It is unclear what type of product this label is attached to or what the purpose of the testing is.*