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'.*

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