Estradiol Tablet
Product Images NDC 0555-0886

View Photos of 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 Estradiol (NDC 0555-0886). 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

Image 1
Chemical structure of Estradiol, the active ingredient depicted in the diagram showing its molecular arrangement including hydroxyl groups and methyl substitution.*
FDA Label Image

Image 2

Image 2
Label for Estradiol Tablets USP 0.5 mg by Teva Pharmaceuticals USA, Inc. The oral tablet packaging indicates a count of 100 tablets. The label includes storage instructions, a barcode, NDC number 0555-0899-02, and a caution to keep the medication out of reach of children.*
FDA Label Image

Image 3

Image 3
Label for Estradiol Tablets USP 1 mg from Teva Pharmaceuticals USA, Inc. The label includes dosage strength of 1 mg per tablet, a barcode, NDC number 0555-0886-02, storage instructions at 20 to 25 degrees Celsius, and a note to dispense with patient information leaflet. Package contains 100 tablets, labeled for prescription use only.*
FDA Label Image

Image 4

Image 4
The label shows Estradiol Tablets USP 2 mg by Teva Pharmaceuticals USA, Inc. It is an oral prescription drug supplied in a 100-tablet package. The label includes dosage and storage instructions, a barcode, and a warning to keep the medication out of children's reach. It indicates inclusion of FD&C Yellow No. 5 as a color additive.*

* 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.