Tpoxx Capsule
Product Images NDC 50072-200

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tpoxx (NDC 50072-200). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Siga Technologies, 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

Tecovirimat Chemical Structure (Tpoxx 01)

Chemical structure of tecovirimat monohydrate showing its detailed molecular arrangement including ring systems, functional groups, and a trifluoromethyl substituent attached to a benzene ring, along with a hydrate (H2O) molecule.*

FDA Label Image

200 mg Capsule 42-count Bottle Label (Tpoxx 02)

Label for TPOXX (tecovirimat) Capsules, 200 mg oral dosage form. The label indicates each capsule contains tecovirimat monohydrate equivalent to 200 mg tecovirimat, with a package count of 42 capsules. Manufactured by Catalent Pharma Solutions for SIGA Technologies, Inc. Storage instructions and safety note to keep out of reach of children are included.*

FDA Label Image

Tpoxx 03

TPOXX (tecovirimat) Injection 200 mg per 20 mL (10 mg/mL) single-dose vial label. The label indicates intravenous infusion use, storage instructions, and distribution by SIGA Technologies, Inc. Includes barcode and NDC 50072-010-30 with directions to dilute before use.*

FDA Label Image

Tpoxx 04

Packaging label for TPOXX (tecovirimat) injection, 200 mg/20 mL (10 mg/mL) for intravenous infusion. The label states 'Dilute Before Use' and indicates the product contains 7 single-dose vials of 20 mL each. Distributed by SIGA Technologies, Inc., Corvallis, OR. Storage instructions specify refrigeration at 2°C to 8°C (36°F to 46°F) with a caution not to freeze.*

* 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.