Amoxicillin And Clavulanate Potassium
Product Images NDC 67296-0123

3 FDA label images from Redpharm Drug, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Amoxicillin And Clavulanate Potassium (NDC 67296-0123). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, Inc., 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

28 (Doc20170419163303 001)

28 (Doc20170419163303 001)
Label for Amoxicillin and Clavulanate Potassium 875/125 mg tablets, prescription only, containing 28 tablets. The label shows the NDC 67296-0123-1, manufacturing by Teva Canada Limited, and distribution by RedPharm Drug, Inc. The lot number, expiration date, storage instructions, and a barcode are also visible.*
FDA Label Image

#6 (Doc20170419163334 001)

#6 (Doc20170419163334 001)
Label for Amoxicillin and Clavulanate Potassium tablets, strength 875 mg/125 mg, packaged as 6 tablets. The label includes NDC 67296-0123-2, with manufacturer Teva Canada Limited and distributor RedPharm Drug, Inc. The label also notes Rx Only status, lot number 26340A2, expiration 07/14, storage instructions, and a barcode.*
FDA Label Image

#14 (Doc20170419163356 001)

#14 (Doc20170419163356 001)
Packaging label for Amoxicillin and Clavulanate Potassium tablets, 875/125 mg strength. The label indicates a quantity of 14 tablets, Rx only, with lot number 26340A 1 and expiration date 07/14. The label shows manufacturing details from Teva Canada Limited, Toronto, Canada, and distribution by RedPharm Drug, Inc. in Eden Prairie, MN. The NDC is 67296-0123-3 and includes a barcode.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.