Fluoxetine Capsule
Product Images NDC 63187-069

3 FDA label images from Proficient Rx Lp · 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 Fluoxetine (NDC 63187-069). 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

63187-081-30 (Fluoxetine Fig1)

63187-081-30 (Fluoxetine Fig1)
Label for Fluoxetine 10 mg capsules by Proficient Rx LP. The label states each capsule contains Fluoxetine hydrochloride USP equivalent to 10 mg fluoxetine in a size 3 opaque green hard gelatin capsule. The label includes lot, expiration information placeholders, and storage instructions. Manufacturer is Aurobindo Pharma Limited, Hyderabad, India.*
FDA Label Image

63187-069-60 (Fluoxetine Fig2)

63187-069-60 (Fluoxetine Fig2)
Fluoxetine 20 mg capsules label by Proficient Rx LP, containing 30 capsules. The label includes a description of the capsule appearance: opaque green cap, opaque off-white body, size '3' hard gelatin capsule filled with off-white granules, imprinted with 'E' on the cap and '91' on the body in black ink. Manufactured by Aurobindo Pharma Limited, Hyderabad, India. Storage instructions specify 20°-25°C (68°-77°F).*
FDA Label Image

Chemical Structure (Fluoxetine Str)

Chemical Structure (Fluoxetine Str)
Chemical structure of Fluoxetine Hydrochloride showing its molecular framework including a trifluoromethyl-substituted phenyl ring linked via an ether bond to a propylamine chain and a phenyl group, with a hydrochloride salt indicated.*

* 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.