Product Images Methocarbamol

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Product Label Images

The following 4 images provide visual information about the product associated with Methocarbamol NDC 36000-302 by Baxter Healthcare Corporation, 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.

carton-03.jpg - carton 03

carton-03.jpg - carton 03

NDC 36000-302-25 is a single-dose vial containing Methocarbamol Injection, which can be given through Intravenous or Intramuscular Injection. This injection is used when necessary and contains Methocarbamol, USP 100 mg; Polyethylene Glycol 300, NF 0.5 mL; and Water for Injection, USP q.s. It should be stored between 20°C to 25°C (68°F to 77°F), with excursions allowed between 15°C to 30°C. There are further instructions where the usage of the product is concerned that should be seen before usage.*

carton-04.jpg - carton 04

carton-04.jpg - carton 04

NDC 36000-302-25 is a Methocarbamol Injection, USP with a concentration of 1,000 mg/10 mL (100 mg/mL) for intravenous or intramuscular injection. This product comes in a package of 25 single-dose vials, each containing 10 mL of solution, which should be discarded if unused. Baxter Healthcare Corporation is the manufacturer of this product and it is manufactured by Gland Pharma Limited in India. The manufacturing plot is located in the Telangana District of Hyderabad. The ML No. is TS/SGY/2019-48573. The AINXOOOOX code and the date of production are not clear from the text.*

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container-02.jpg - container 02

This is a product description for Methocarbamol Injection, USP, which comes in a 10 mL single-dose vial with 1,000 mg/10 mL concentration (100 mg/mL) for intravenous or intramuscular injection. It is used to relieve muscle pain and discomfort caused by Musculoskeletal conditions. Each mL of the injection contains Methocarbamol, USP (100 mg), Polyethylene Glycol 300, NF (0.5 mL), Water for Injection, USP q.s. pH adjusted with hydrochloric acid and/or sodium hydroxide. The injection should not be refrigerated after mixing with intravenous infusion fluids. The label provides detailed directions for use and storage of the product.*

structure-01 - structure 01

structure-01 - structure 01

* 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.