Labetalol Hydrochloride Tablet, Film Coated
Product Images NDC 51655-322

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Labetalol Hydrochloride (NDC 51655-322). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

51655-322-25 (51655 322 25 Rev A 04 23)

51655-322-25 (51655 322 25   Rev A 04 23)
This is a description of a medication called Labetalol Hydrochloride Tablets, USP. Each tablet contains 100mg of labetalol hydrochloride. The medication is packaged in a container with 60 tablets. It is only available with a prescription. The recommended dosage can be found in the package insert. The medication should be stored at a temperature between 20° - 25°C (68° - 77°F), following the USP Controlled Room Temperature guidelines. It is important to keep the medication out of the reach of children and store it in its original container, tightly closed. The medication has been repackaged by Northwind Pharmaceuticals, located in Indianapolis, IN 46203. The original manufacturer of the medication is Biocon Pharma Inc., and the lot number of the medication is 0000000000. The medication is repackaged from a product with NDC number 70377-060-XX and has a GTIN number of 00351655322253. The expiration date of the medication is 00/00/0000.*
FDA Label Image

Chem Structure (Chemstructure)

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