Oseltamivir Phosphate Capsule
Product Images NDC 67296-1940

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oseltamivir Phosphate (NDC 67296-1940). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Oseltamivir-02 (Oseltamivir 02)

Packaging label for Oseltamivir Phosphate Capsules USP 30 mg by Lannett Company, Inc. The label states the product contains 10 capsules, includes storage instructions, and notes the capsules contain oseltamivir phosphate equivalent to 30 mg oseltamivir free base. The label includes the NDC 0527-4591-13 and manufacturer Sunshine Lake Pharma Co., Ltd., Guangdong Province, China.*

FDA Label Image

Oseltamivir-03 (Oseltamivir 03)

Packaging label for Oseltamivir Phosphate capsules, USP, showing the 45 mg strength. The label indicates the product contains 10 capsules per package. It includes storage instructions, manufacturer (Sunshine Lake Pharma Co., Ltd., China), and distributor information (Lannett Company, Inc., Philadelphia, PA). The design features the Lannett logo and barcode.*

FDA Label Image

Oseltamivir-04 (Oseltamivir 04)

Packaging label for Oseltamivir Phosphate Capsules USP, 75 mg, oral capsules. The label indicates a package of 10 capsules, distributed by Lannett Company, Inc., and manufactured by Sunshine Lake Pharma Co., Ltd. The label includes storage instructions and a barcode, with branding from Lannett and HEC logos.*

FDA Label Image

Chemical Structure (Tamiflu 01)

Chemical structure of oseltamivir phosphate depicted as a molecular diagram illustrating its key functional groups and stereochemistry.*

* 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.