Cefdinir Powder, For Suspension
Product Images NDC 72189-259

4 FDA label images from Direct Rx · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Cefdinir (NDC 72189-259). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

04332 (043 32)

04332 (043 32)
Label for CEFDINIR oral suspension 250 mg/5 mL, powder for suspension in a 100 mL bottle. It is a generic for OMNICEF and is packaged and distributed by DIRECT RX. The label includes dosage strength, volume, lot number, expiration date, and NDC numbers for the product.*
FDA Label Image

72189 0185 32

72189 0185 32
Label for CEFDINIR ORAL SUSPENSION 125 mg/5 mL in a 100 mL container. The label states it is generic for Omnicef, with each 5 mL of reconstituted suspension containing 125 mg of Cefdinir USP. It shows the NDC 72189-185-32, lot number 08MA2112, and an expiration date of 03/31/22. The product is packaged and distributed by Direct Rx.*
FDA Label Image

72189 0259 32

72189 0259 32
CEFDINIR ORAL SUSP 250 mg/5 mL powder for suspension in a 100 mL bottle. The label indicates it is a generic form of Omnicef with each 5 mL containing 250 mg of cefdinir. The product is packaged and distributed by Direct RX, with lot and expiration dates printed on the label.*
FDA Label Image

72189 186 32

72189 186 32
Packaging label for CEFDINIR ORAL SUSP 250 mg/5 mL powder for suspension, 100 mL bottle. It is a generic form of OMNICEF, containing 250 mg of cefdinir per 5 mL of reconstituted oral suspension. The label includes the NDC 72189-186-32 and is distributed by DIRECT RX.*

* 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.