Clomiphene Citrate Tablet
Product Images NDC 83390-107

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Clomiphene Citrate (NDC 83390-107). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cosette Pharmaceuticals Nc Laboratories, Llc, 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

This Is The Structural Formula (Clomiphene Citrate Tablets 1)

This Is The Structural Formula (Clomiphene Citrate Tablets 1)
Chemical structure of Clomiphene Citrate showing its molecular arrangement including aromatic rings and the citrate component.*
FDA Label Image

50mg/10 Tablets (carton)

50mg/10 Tablets (carton)
Packaging label for Clomiphene Citrate Tablets, USP 50 mg, by Myriel Pharmaceuticals. The label shows the product name and strength prominently, with a count of 10 tablets per package. It includes dosage form as oral tablets and states Rx only. Storage and usage instructions, barcode, and distributor info for Myriel Pharmaceuticals are also present.*
FDA Label Image

50mg/30 Tablets Carton (Clomiphene Citrate Tablets 5)

50mg/30 Tablets Carton (Clomiphene Citrate Tablets 5)
The packaging label for ClomiPHENE Citrate Tablets, USP 50 mg is shown. The label indicates oral tablets with 30 tablets per container. The label includes warnings to keep out of reach of children and storage instructions. Distributed by Myriel Pharmaceuticals LLC. The design features the product name prominently with dosage strength and includes a barcode and the Myriel Pharmaceuticals logo.*

* 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.