Fluoxetine Hydrochloride Tablet, Coated
Product Images NDC 49884-335

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Fluoxetine Hydrochloride (NDC 49884-335). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Par Health Usa, Llc, 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 (Fluoxetine Hydrochloride Tablet 1)

Chemical structure of fluoxetine hydrochloride, showing the molecular arrangement of atoms including trifluoromethyl group, aromatic rings, ether linkage, and hydrochloride component.*

FDA Label Image

Fluoxetine (Fluoxetine Hydrochloride Tablet 2)

Fluoxetine Tablets, USP 10 mg coated tablets label from Par Pharmaceutical. The label states each tablet contains 10 mg fluoxetine as fluoxetine hydrochloride. It includes dispensing instructions, storage conditions (20° to 25°C), package size of 30 tablets, and manufacturer information (Par Formulations Private Limited, India). The label also features the NDC number 49884-335-11 and a barcode.*

FDA Label Image

Fluoxetine (Fluoxetine Hydrochloride Tablet 3)

Fluoxetine Tablets USP 10 mg coated tablets label for prescription use. Contains 100 tablets per container. Distributed by Par Pharmaceutical, manufactured by Par Formulations Private Limited in India. Instructions include storage at 20° to 25°C and dispensing with medication guide to each patient.*

FDA Label Image

Fluoxetine (Fluoxetine Hydrochloride Tablet 4)

Fluoxetine Tablets USP 10 mg film-coated tablets label by Par Health USA, LLC. The label indicates each tablet contains 10 mg fluoxetine hydrochloride. Packaging contains 1,000 tablets. Instructions note dispensing with medication guide, storage at 20° to 25°C, and protection from light. Distributed by Par Pharmaceutical in the USA and manufactured by Par Formulations Private Limited in India.*

FDA Label Image

Fluoxetine (Fluoxetine Hydrochloride Tablet 5)

Label for Fluoxetine Tablets USP 20 mg oral coated tablets, supplied in a package of 30 tablets by Par Pharmaceutical. The label includes dosage information, storage instructions, and safety warnings, and features the NDC 49884-336-11 and barcode.*

FDA Label Image

Fluoxetine (Fluoxetine Hydrochloride Tablet 6)

Fluoxetine Tablets, USP 20 mg film-coated tablets, oral dosage form, in a 100-tablet package. The label includes dispensing instructions, storage conditions (20° to 25°C), and manufacturer information for Par Pharmaceutical and Par Formulations Private Limited. The label also features an NDC barcode and a website address for medication guides.*

FDA Label Image

Fluoxetine (Fluoxetine Hydrochloride Tablet 7)

Fluoxetine Tablets, USP 20 mg film-coated oral tablets label showing a quantity of 1,000 tablets. The label indicates the active ingredient as fluoxetine hydrochloride 20 mg per tablet. It includes dispensing instructions for pharmacists, storage conditions, and manufacturer details for Par Pharmaceutical USA and Par Formulations Private Limited, India. The label also displays a barcode and the NDC 49884-336-10.*

* 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.