Fluoxetine
Product Images NDC 31722-905

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fluoxetine (NDC 31722-905). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber Pharmaceuticals, 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

Fluoxetine10mg30s (Fluoxetine10mg30s)

Fluoxetine Capsules, USP 10 mg label from Camber Pharmaceuticals, Inc. The label shows dosage of 10 mg per capsule, the NDC 31722-903-30, barcode, lot and expiration fields, storage instructions, pharmacist dispensing note, contact number, and manufacturer information. Package contains 30 capsules, prescription only.*

FDA Label Image

Fluoxetine20mg30s (Fluoxetine20mg30s)

Fluoxetine Capsules, USP 20 mg by Camber Pharmaceuticals, Inc. The label shows NDC 31722-904-30 and indicates a package size of 30 capsules. It includes storage instructions and contact information for the manufacturer and labeler. The barcode and lot/expiration placeholders are visible.*

FDA Label Image

Fluoxetine40mg30s (Fluoxetine40mg30s)

Fluoxetine Capsules, USP 40 mg label from Camber Pharmaceuticals, Inc. The label includes dosage instruction advisories, child-resistant container dispensation guidance, storage temperature ranges, and manufacturer information. The package contains 30 capsules with an NDC number 31722-905-30 and a barcode.*

FDA Label Image

Fluoxetinestructure (Fluoxetinestructure)

Chemical structure of fluoxetine hydrochloride, showing the molecular arrangement including a trifluoromethyl group on a benzene ring, connected through an ether linkage to a side chain with an amine group and a phenyl ring, associated with hydrochloride.*

* 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.