Cefdinir Capsule
Product Images NDC 67877-543

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Cefdinir (NDC 67877-543). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ascend Laboratories, Llc, 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

Cefdinir 300mg 100cap Cart

Folded carton label for Cefdinir Capsules USP, 300 mg, by Ascend Laboratories, LLC. The label indicates the product contains 100 unit dose capsules, not a child-resistant pack, Rx only. Manufactured by Alkem Laboratories Ltd., India, distributed by Ascend Laboratories in Parsippany, NJ. Storage instructions and usual dosage notes are visible.*

FDA Label Image

Cefdinir 300mg 100cap

Label for Cefdinir capsules, USP 300 mg by Ascend Laboratories, LLC. The label states the capsule strength as 300 mg, the quantity of 100 capsules, and includes storage instructions between 20° to 25°C. It displays the NDC number 67877-543-01 and notes the product is Rx Only. Manufacturer is Alkem Laboratories Ltd., India, with distribution by Ascend Laboratories in Parsippany, NJ.*

FDA Label Image

Cefdinir 300mg 60cap

Label for Cefdinir Capsules, USP 300 mg oral capsules by Ascend Laboratories, LLC. The package contains 60 capsules and includes storage instructions (20° to 25°C) and a note to keep out of reach of children. Manufactured by Alkem Laboratories, Ltd., India. The NDC is 67877-543-60.*

FDA Label Image

Cefdinir-structure (Cefdinir Structure)

Chemical structure diagram of the active ingredient cefdinir, showing its molecular framework with atoms and bonds clearly represented.*

* 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.