Product Images Famotidine

View Photos of Packaging, Labels & Appearance

Product Label Images

The following 2 images provide visual information about the product associated with Famotidine NDC 51655-553 by Northwind Pharmaceuticals, 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.

Label - 51655 553 52 Master Bottle Label Approval Rev A 07 21

Label - 51655 553 52 Master Bottle Label Approval   Rev A 07 21

NDC number 51655-553-52 identifies a batch of 30 Famotidine Tablets USP (20 mg) that requires a valid prescription to purchase. The tablets are film-coated and contain Famotidine USP 20mg. Follow the dosage mentioned in the package insert and store them at USP Controlled Room Temperature. These tablets have been repackaged by Northwind Pharmaceuticals with a new Standard Identification Number (SIN). The original manufacturer, Aurobindo Pharma USA, Inc, is identified by the Repackaged From number 65862-859-XX, and the expiry date and lot number are listed as 00/00/0000 and 0000000000, respectively. Keep the tablets out of children's reach and store in the original container.*

str1 - famotidine str

str1 - famotidine str

* 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.