Oseltamivir Phosphate Capsule
Product Images NDC 71205-206

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 Oseltamivir Phosphate (NDC 71205-206). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Image 1 (27423baa 8d58 48c3 8ee1 069e848669e4 01)

Image 1 (27423baa 8d58 48c3 8ee1 069e848669e4 01)
Chemical structure of Oseltamivir phosphate, showing molecular bonds and functional groups including ester, amine, and phosphate components.*
FDA Label Image

Image09 (27423baa 8d58 48c3 8ee1 069e848669e4 02)

Image09 (27423baa 8d58 48c3 8ee1 069e848669e4 02)
An instructional diagram showing three steps to access capsules from a blister pack. Steps include tearing along the perforation to separate, peeling the paper to expose the foil, and pushing the capsule through the foil, using hand illustrations.*
FDA Label Image

71205-206-10 (27423baa 8d58 48c3 8ee1 069e848669e4 03)

71205-206-10 (27423baa 8d58 48c3 8ee1 069e848669e4 03)
Label for Oseltamivir Phosphate 75 mg capsules by Proficient Rx LP, a human prescription drug. The label indicates a package of 10 capsules, each containing oseltamivir phosphate equivalent to 75 mg oseltamivir free base. Capsules are size 2 hard gelatin with a light yellow cap and grey opaque body, imprinted with '75 mg' and 'LU'. Manufactured by Lupin Limited in India. Includes storage instruction to keep at 25°C and a warning to keep medication out of children's reach.*

* 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.