Hydrocortisone Tablet
Product Images NDC 71930-078

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydrocortisone (NDC 71930-078). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eywa 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

10mg (10mg)

Hydrocortisone Tablets USP 10 mg oral tablets label from Eywa Hibrow Pharma. The label includes storage instructions, a warning that the drug must be used under physician supervision, dosage information stating each tablet contains 10 mg hydrocortisone, and the number of tablets (100). It is distributed by Eywa-Hibrow Pharma in New Jersey and made in India.*

FDA Label Image

20mg (20mg)

Label for hydrocortisone tablets, USP 20 mg oral tablets by Eywa Pharma Inc. The label states NDC 71930-080-12 and indicates a quantity of 100 tablets. Storage instructions and usage warnings are provided. The product is distributed by Eywa-Hibrow Pharma, made in India, with related regulatory information shown.*

FDA Label Image

5mg (5mg)

Hydrocortisone Tablets USP 5 mg oral tablets label from Eywa-Hibrow Pharma. The label includes storage instructions, usage warnings, dosage information, and distributor details. It states each tablet contains 5 mg hydrocortisone and comes in a bottle of 50 tablets. The product is made in India.*

FDA Label Image

Str (Struct)

Chemical structure diagram depicting hydrocortisone, showing its complex steroid skeleton with labeled functional groups including hydroxyl (OH) and carbonyl (CO) groups, methyl (CH3) substitutions, and various hydrogen atoms.*

* 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.