Fluoxetine Capsule
Product Images NDC 50090-2589

3 FDA label images from A-s Medication Solutions · 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 50090-2589). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Fluoxetine Str)

Chemical Structure (Fluoxetine Str)
Chemical structure diagram of Fluoxetine hydrochloride, showing the molecular arrangement including a trifluoromethyl-substituted aromatic ring, an ether linkage to a phenyl-ethylamine moiety, and the hydrochloride salt component.*
FDA Label Image

Label Image (Lbl500902589)

Label Image (Lbl500902589)
Label for Fluoxetine 40 mg capsules by A-S Medication Solutions. The label shows product number 5320-0 and NDC 50090-2589-0. It states that each capsule contains fluoxetine hydrochloride USP equivalent to 40 mg of fluoxetine. Storage instructions advise keeping the product at 68 to 77 degrees Fahrenheit. The package contains 30 capsules and includes a QR code. The labeler is located in Libertyville, IL 60048.*
FDA Label Image

Label Image (Lbl500902793)

Label Image (Lbl500902793)
Fluoxetine 40 mg capsule label from A-S Medication Solutions. The label states each capsule contains fluoxetine hydrochloride equivalent to 40 mg of fluoxetine. Storage instructions indicate to keep at 68 to 77 degrees Fahrenheit. The container holds 32 unit dose capsules, and includes a QR code for dosage information.*

* 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.