Spectracef
Product Images NDC 44004-801

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Spectracef (NDC 44004-801). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vansen Pharma 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

Spectracef 200 mg (Spectracef 200mg Label)

Packaging label for Spectracef 200 mg tablets by Vansen Pharma Inc. The box is designed for a 20-tablet dose pack of cefditoren pivoxil tablets. The label features blue and white colors with the product name prominently displayed and dosage information included. The label also states "Rx Only" and includes a barcode and NDC number 4400-4801-20.*

FDA Label Image

Spectracef 400mg- 20pack (Spectracef 400mg Label 20pack)

Packaging label for Spectracef 400 mg tablets, a 20-tablet dose pack of cefditoren pivoxil. The box is predominantly blue and white with orange accents, labeled for prescription use only by Vansen Pharma Inc. Storage instructions and tamper-evident warnings are visible.*

FDA Label Image

Spectracef 400 mg- 28pack (Spectracef 400mg Label 28pack)

Packaging label for Spectracef 400 mg Tablets by Vansen Pharma Inc. The label indicates a 28-tablet dose pack of cefditoren pivoxil, with instructions to keep medication out of children's reach and storage temperature guidance. It is marked Rx Only and displays Vansen Pharma Inc. as the labeler.*

FDA Label Image

Cefditoren Pivoxil (Spectracef 1)

Chemical structure of the active ingredient in Spectracef, illustrating a complex molecular formula with distinct functional groups and rings, including heteroatoms such as nitrogen, oxygen, sulfur, and methyl substituents.*

* 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.