Fluoxetine Hydrochloride
Product Images NDC 67046-211

3 FDA label images from Contract Pharmacy Services-pa · 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 Hydrochloride (NDC 67046-211). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Contract Pharmacy Services-pa, 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

Fluoxetine Hydrchloride (4e4d8017 9c1d 41eb Affb 8046e3548be9 01)

Fluoxetine Hydrchloride (4e4d8017 9c1d 41eb Affb 8046e3548be9 01)
Chemical structure diagram of Fluoxetine Hydrochloride, showing its molecular configuration with aromatic rings and functional groups.*
FDA Label Image

Logo (4e4d8017 9c1d 41eb Affb 8046e3548be9 02)

Logo (4e4d8017 9c1d 41eb Affb 8046e3548be9 02)
Fluoxetine Hydrochloride 20 mg capsules in a white and blue blister pack. The packaging includes 30 capsules and shows the labeler as Contract Pharmacy Services-PA. The capsules are blue and white, with the imprint '674' visible on the blue half.*
FDA Label Image

Blister Of 30 (4e4d8017 9c1d 41eb Affb 8046e3548be9 03)

Blister Of 30 (4e4d8017 9c1d 41eb Affb 8046e3548be9 03)
Packaging label for Fluoxetine Hydrochloride 20 mg capsules, quantity 30, labeled by Contract Pharmacy Services-PA. The label includes dosage and storage instructions, a barcode, lot number labeled as 'SAMPLE', expiration date 03/11, and a 30-day pill organizer layout numbered 1 to 30 for daily medication tracking.*

* 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.