Amoxicillin And Clavulanate Potassium Powder, For Suspension
Product Images NDC 0093-2279

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Amoxicillin And Clavulanate Potassium (NDC 0093-2279). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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

Image 1

Chemical structure of Amoxicillin and Clavulanate Potassium, showing molecular bonds and atoms, including phenol, amide, beta-lactam, and other functional groups, along with associated water molecules (3H2O).*

FDA Label Image

Image 2

Chemical structure of Amoxicillin and Clavulanate Potassium, showing the molecular arrangement of its components including the beta-lactam ring and functional groups relevant to its antibiotic activity.*

FDA Label Image

Image 3

Label for Amoxicillin and Clavulanate Potassium Tablets USP, 500 mg/125 mg strength, oral film-coated tablets. The label shows the product name, strength, dosage form, a count of 20 tablets, and the manufacturer Teva Pharmaceuticals USA, Inc. It includes NDC 0093-2274-34 and storage and usage instructions on the back. The label also features a barcode and spaces for lot number and expiration date.*

FDA Label Image

Image 4

Label for Amoxicillin and Clavulanate Potassium Tablets USP, 875 mg/125 mg strength. The label indicates the product is prescription only and contains 20 film-coated tablets. It is produced by Teva Pharmaceuticals USA, Inc. Additional information includes the NDC number 0093-2275-34, barcodes, and areas designated for lot and expiration dates.*

FDA Label Image

Image 5

Label for Amoxicillin and Clavulanate Potassium Oral Suspension USP 200 mg/28.5 mg per 5 mL by Teva Pharmaceuticals USA, Inc. The label includes dosage strength information, reconstitution instructions, and storage instructions. The package contains 100 mL of suspension when reconstituted.*

FDA Label Image

Image 6

Label for Amoxicillin and Clavulanate Potassium Oral Suspension USP 400 mg/57 mg per 5 mL by Teva Pharmaceuticals USA, Inc. It is a 100 mL bottle when reconstituted. The label includes dosage details, preparation instructions, and the NDC code 0093-2279-73, stating it is for Rx only.*

FDA Label Image

Image 7

Label for Amoxicillin and Clavulanate Potassium chewable tablets USP, strength 200 mg/28.5 mg, manufactured by Teva Pharmaceuticals USA, Inc. The label includes drug information such as contents of each chewable tablet, lot and expiration date fields, and indicates prescription use only. The package contains 20 chewable tablets.*

FDA Label Image

Image 8

Label for Amoxicillin and Clavulanate Potassium Tablets USP, chewable, 400 mg/57 mg strength. The label indicates the product is supplied by Teva Pharmaceuticals USA, Inc. It also states the package contains 20 chewable tablets, with lot and expiration date fields, and the drug is for prescription use only.*

* 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.