Fluoxetine Capsule
Product Images NDC 71209-040

12 FDA label images from Cadila Pharmaceuticals Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Fluoxetine (NDC 71209-040). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cadila 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.

FDA Label Image

Fluoxetine-spl-10mg-100.jpg (Fluoxetine Spl 10mg 100)

Fluoxetine-spl-10mg-100.jpg (Fluoxetine Spl 10mg 100)
Fluoxetine capsules USP 10 mg oral dosage form, presented in a label showing 100 capsules per container. The label includes storage instructions, manufacturer details (Cadila Pharmaceuticals Limited, Gujarat, India), and a barcode. The label prominently displays the strength as 10 mg and states 'Rx only.'*
FDA Label Image

Fluoxetine-spl-10mg-1000.jpg (Fluoxetine Spl 10mg 1000)

Fluoxetine-spl-10mg-1000.jpg (Fluoxetine Spl 10mg 1000)
Fluoxetine Capsules, USP 10 mg oral capsules label by Cadila Pharmaceuticals Limited. The label states each capsule contains fluoxetine hydrochloride equivalent to 10 mg fluoxetine. Packaging highlights 1000 capsules in a light-resistant container with a barcode and storage instructions at 20° to 25°C. The product is prescription-only and includes a medication guide advisory for pharmacists.*
FDA Label Image

Fluoxetine-spl-10mg-30.jpg (Fluoxetine Spl 10mg 30)

Fluoxetine-spl-10mg-30.jpg (Fluoxetine Spl 10mg 30)
Fluoxetine Capsules, USP 10 mg oral capsules label from Cadila Pharmaceuticals Limited. The label shows 30 capsules per container with prescription use only. It includes storage instructions, manufacturer address in Gujarat, India, and a barcode on a white background with red and beige design elements.*
FDA Label Image

Fluoxetine-spl-10mg-500.jpg (Fluoxetine Spl 10mg 500)

Fluoxetine-spl-10mg-500.jpg (Fluoxetine Spl 10mg 500)
Label for Fluoxetine Capsules, USP 10 mg oral capsules by Cadila Pharmaceuticals Limited. The label indicates a package size of 500 capsules and includes storage instructions, NDC 71209-040-10, and a barcode. It states that each capsule contains fluoxetine hydrochloride equivalent to 10 mg fluoxetine, labeled Rx only.*
FDA Label Image

Fluoxetine-spl-20mg-100 (Fluoxetine Spl 20mg 100)

Fluoxetine-spl-20mg-100 (Fluoxetine Spl 20mg 100)
Fluoxetine Capsules, USP 20 mg oral capsules label by Cadila Pharmaceuticals Limited. The label shows the quantity of 100 capsules with Rx only designation. It includes storage instructions, manufacturing details from Ahmedabad, Gujarat, India, and a barcode. The label features design elements in brown and white, with details about dosage and packaging.*
FDA Label Image

Fluoxetine-spl-20mg-1000.jpg (Fluoxetine Spl 20mg 1000)

Fluoxetine-spl-20mg-1000.jpg (Fluoxetine Spl 20mg 1000)
Label for Fluoxetine Capsules USP, 20 mg, oral capsule form, containing 1000 capsules. The label includes storage instructions, manufacturer information (Cadila Pharmaceuticals Ltd, Ahmedabad, India), and a note to pharmacists to dispense the medication guide with the product. The NDC number 71209-041-11 is displayed along with barcode.*
FDA Label Image

Fluoxetine-spl-20mg-30 (Fluoxetine Spl 20mg 30)

Fluoxetine-spl-20mg-30 (Fluoxetine Spl 20mg 30)
Fluoxetine Capsules, USP 20 mg oral capsule label by Cadila Pharmaceuticals Limited. The label states the NDC as 71209-041-01 and indicates a package quantity of 30 capsules. It includes storage instructions, dosage form, and manufacturer details with a barcode and areas for serialized datamatrix code and batch coding.*
FDA Label Image

Fluoxetine-spl-20mg-500.jpg (Fluoxetine Spl 20mg 500)

Fluoxetine-spl-20mg-500.jpg (Fluoxetine Spl 20mg 500)
Fluoxetine Capsules USP 20 mg oral capsules label from Cadila Pharmaceuticals Limited. The label indicates a package size of 500 capsules and includes storage instructions, dispensing guidance, and a barcode. It also provides the manufacturing license number and the manufacturer's address in Gujarat State, India.*
FDA Label Image

Fluoxetine-spl-40mg-100.jpg (Fluoxetine Spl 40mg 100)

Fluoxetine-spl-40mg-100.jpg (Fluoxetine Spl 40mg 100)
Label for Fluoxetine Capsules, USP 40 mg by Cadila Pharmaceuticals Limited. The label indicates a package containing 100 capsules, with instructions for dispensing and storage. It includes the NDC 71209-042-05 and details that each capsule contains fluoxetine hydrochloride equivalent to 40 mg fluoxetine. The label notes it is for Rx only and includes manufacturing information from Gujarat State, India.*
FDA Label Image

Fluoxetine-spl-40mg-500 (Fluoxetine Spl 40mg 30)

Fluoxetine-spl-40mg-500 (Fluoxetine Spl 40mg 30)
Label for Fluoxetine Capsules, USP 40 mg by Cadila Pharmaceuticals Limited. The label indicates each capsule contains fluoxetine hydrochloride equivalent to 40 mg of fluoxetine. The package contains 30 capsules. Storage instructions and barcode are also visible.*
FDA Label Image

Fluoxetine-spl-40mg-500.jpg (Fluoxetine Spl 40mg 500)

Fluoxetine-spl-40mg-500.jpg (Fluoxetine Spl 40mg 500)
Fluoxetine Capsules, USP 40 mg oral capsules packaging label by Cadila Pharmaceuticals Limited. The label indicates a bottle count of 500 capsules, with storage instructions, prescription-only status, and a note for pharmacists to dispense the enclosed medication guide. It includes the NDC code 71209-042-10 and manufacturer information from India.*
FDA Label Image

Fluoxetine-spl-stru-fig1 (Fluoxetine Spl Stru Fig1)

Fluoxetine-spl-stru-fig1 (Fluoxetine Spl Stru Fig1)
Chemical structure of Fluoxetine hydrochloride, showing the molecular arrangement of its components including a trifluoromethyl group, phenyl rings, and an amine hydrochloride moiety.*

* 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.