Product Images Glycopyrrolate
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Product Label Images
The following 7 images provide visual information about the product associated with Glycopyrrolate NDC 51662-1487 by Hf Acquisition Co Llc, Dba Healthfirst, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.
POUCH LABELING - 51662 1487 2 POUCH LABELING
Glycopyrrolate Injection is a medication available in a 0.2mg/mL solution and is sold in 1mL vials containing benzyl alcohol. The medication is not suitable for newborns and users should refer to the package insert for the appropriate dosage recommendations. The medication should be stored within a temperature range of 20°C to 25°C (68°F to 77°F). The medication is intended for intramuscular or intravenous use only. The product's lot number is 1234586 and has an expiry date of 2030-01:-01. The NDC code of the product is 51662-1487-2, and the original manufacturer's code is 0143-9682-25.*
BOX LABELING - 51662 1487 3 BOX LABELING
Glycopyrrolate Injection, USP 0.2mg/mL with Benzyl Alcohol is a medication used for IM or IV use, typically stored at 20-25°C (68-77°F). This injection should not be used in newborns and its usual dosage is provided in the package insert. The product comes in a 1mL vial box of 25, and the lot number is 123456 with an expiration date of 2030-01-0Q1. The product's NDC is 31662-1487-3, and its RX Only label indicates that it must be distributed and sold under a licensed healthcare provider's supervision. The manufacturer is HF Acquisition Co., LLC, and its original NDC is 0143-9682-25.*
SERIALIZED BOX LABELING - 51662 1487 3 SERIALIZED LABELING
CLINICAL - CLINICAL PHARMA
SERIALIZED LABELING - SERIALIZED VIAL LABELING
STRUCTURE - STRUCTURE
VIAL LABEL - VIAL LABEL
This is a label of a single dose vial of Glycopyrrolate, a medication that can be used through intramuscular or intravenous administration. This medication's concentration is 0.2 mg/mL, and it contains benzyl alcohol. The label shows the National Drug Code (NDC) number, the manufacturer's name (Westward), and a lot number, but the expiration date is not readable.*
* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.