Amoxicillin And Clavulanate Potassium
Product Images NDC 67296-0123

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)

This is a prescription drug with the name "Amoxicillin & Clavulanate Potassium" manufactured by Teva Canada Limited. Each tablet contains 875 mg of Amoxicillin and 125 mg of Clavulanate Potassium. It comes in a bottle containing 28 tablets with lot number 37217A 1 and an expiration date of 08/18. The usual adult dosage is provided in the package insert. It should be stored at a controlled room temperature of 20-25°C (68-77°F). The drug is distributed by Redpharm Drug in Eden Prairie, MN under the NDC number 67296-0123-1.*

FDA Label Image

#6 (Doc20170419163334 001)

This is the information of a medication with the national drug code of 67296-0123-2. The medicine contains amoxicillin and clavulanate potassium and comes in the form of mowy ez. The lot number for this product is 26340A 2 with an expiration date of 07/14. The usual adult dosage is not provided, and the medication must be stored at 20-25 Celsius. The manufacturer of this medication is Teva Canada Limited in Toronto, Canada, and the distributor is Redpharm Drug Eden Prairie in MN 55344. LCN is 391386.*

FDA Label Image

#14 (Doc20170419163356 001)

This is a prescription medication with the NDC code 67296-0123-3, containing Amoxicillin and Clavulanate Potassium, with a strength of 875/125mg. It is manufactured by Teva Canada Limited, located in Toronto, and distributed by Redpharm Drug in Eden Prairie, MN. It also includes the drug name 'VULANATE' and the identification number 'LCN: 391384'.*

* 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.