Fluoxetine Hydrochloride Tablet, Film Coated
Product Images NDC 46708-243

3 FDA label images from Alembic Pharmaceuticals Limited · 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 46708-243). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals Limited, 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

30's Bottle Pack (Fluoxetine mg10)

30's Bottle Pack (Fluoxetine mg10)
Fluoxetine Hydrochloride 10 mg film-coated tablets label from Alembic Pharmaceuticals Limited. The label includes dosing instructions, storage conditions, and a barcode. The package contains 30 tablets and is for oral use. The product is prescription-only and includes pharmacist dispensing guidance.*
FDA Label Image

30's Bottle Pack (Fluoxetine mg20)

30's Bottle Pack (Fluoxetine mg20)
Fluoxetine Hydrochloride 20 mg film-coated tablets packaging label by Alembic Pharmaceuticals Limited. The label includes dosage form, strength, quantity (30 tablets), and storage instructions. It emphasizes dispensing with medication guide and professional prescription use. The label also features the NDC 46708-243-30 and manufacturer details in Gujarat, India.*
FDA Label Image

Structure (Fluoxetine Str)

Structure (Fluoxetine Str)
Chemical structure of Fluoxetine Hydrochloride, showing its molecular composition including a trifluoromethyl-substituted aromatic ring, an ether linkage, and an amine side chain as part of the hydrochloride salt.*

* 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.