Fludrocortisone Acetate Tablet
Product Images NDC 71930-088

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fludrocortisone Acetate (NDC 71930-088). 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

1000s (1000s)

Fludrocortisone Acetate Tablets USP 0.1 mg label for 1000 tablets by Eywa Pharma Inc. The label includes storage instructions, dosage strength, distribution details, and a barcode. It specifies the drug is prescription only and includes a warning about handling and storage conditions, indicating it is made in India.*

FDA Label Image

100s (100s)

Label for Fludrocortisone Acetate Tablets, USP, containing 0.1 mg oral tablets, supplied in a bulk package of 100 tablets. The label identifies Eywa Hibrow Pharma as the distributor and includes storage instructions, dosage information, a barcode, and manufacturing details showing it is made in India.*

FDA Label Image

500s (500s)

Fludrocortisone Acetate Tablets USP 0.1 mg oral tablet label from Eywa Hibrow Pharma. The bulk package contains 500 tablets. The label includes dosage, storage instructions, and manufacturer details, with an NDC of 71930-088-52 and a barcode on the left.*

FDA Label Image

Structure (Structure)

Chemical structure of fludrocortisone acetate showing carbon rings with attached functional groups including hydroxyl, acetoxy, methyl, and fluorine substituents, with stereochemistry indicated by wedge and dashed bonds.*

* 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.