Citalopram Tablet, Film Coated
Product Images NDC 65862-005

10 FDA label images from Aurobindo Pharma Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Citalopram (NDC 65862-005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Package Label-principal Display Panel (10 mg (30 Tablets Bottle))

Package Label-principal Display Panel (10 mg (30 Tablets Bottle))
Packaging label for Citalopram Tablets USP 10 mg film-coated tablets by Aurobindo Pharma Limited. The label is marked Rx only and contains 30 tablets. It includes storage instructions, distributor information for Aurobindo Pharma USA, Inc., and cautionary statements about dispensing and keeping the medication away from children. The label features a designated coding and overprinting zone.*
FDA Label Image

Package Label-principal Display Panel (10 mg Blister Carton (10 x 10 Unit-dose))

Package Label-principal Display Panel (10 mg Blister Carton (10 x 10 Unit-dose))
Packaging label for Citalopram Tablets, USP 10 mg, film-coated tablets by Aurobindo Pharma Limited. The label shows a carton designed to hold 10 x 10 (100) unit dose tablets. It includes the NDC 65862-005-10 and messaging instructing pharmacists to dispense with a medication guide. The active ingredient is citalopram hydrobromide equivalent to 10 mg citalopram base per tablet.*
FDA Label Image

Package Label-principal Display Panel (10 mg Unit-of-Use Pack (30 Tablets))

Package Label-principal Display Panel (10 mg Unit-of-Use Pack (30 Tablets))
Packaging label for Citalopram Tablets, USP 10 mg, film-coated tablets, by Aurobindo Pharma Limited. The label indicates this is a prescription drug with a NDC code 65862-005-32 containing 30 tablets. Instructions for dispensing with a medication guide are also noted. The label features a green and white color scheme with dosage instructions for a blister pack format.*
FDA Label Image

Package Label-principal Display Panel (20 mg (30 Tablets Bottle))

Package Label-principal Display Panel (20 mg (30 Tablets Bottle))
Label for Citalopram Tablets USP 20 mg film-coated tablets from Aurobindo Pharma Limited. The label states the NDC 65862-006-30 and indicates a quantity of 30 tablets. It includes storage instructions (20 to 25°C), dispensing information, and distributor details for Aurobindo Pharma USA, Inc. The label also notes that the product is made in India and features a barcode on the right side.*
FDA Label Image

Package Label-principal Display Panel (20 mg Blister Carton (10 x 10 Unit-dose))

Package Label-principal Display Panel (20 mg Blister Carton (10 x 10 Unit-dose))
Packaging label for Citalopram Tablets, USP 20 mg, film-coated tablets by Aurobindo Pharma Limited. The label indicates 10 x 10 (100) unit dose tablets, specifying the active ingredient as citalopram hydrobromide equivalent to 20 mg citalopram base. The label includes NDC 65862-006-10 and a note to dispense with a medication guide.*
FDA Label Image

Package Label-principal Display Panel (20 mg Unit-of-Use Pack (30 Tablets))

Package Label-principal Display Panel (20 mg Unit-of-Use Pack (30 Tablets))
Packaging label for Citalopram Tablets USP 20 mg film-coated tablets by Aurobindo Pharma Limited. The label features the drug name, strength, quantity of 30 tablets, and pharmacy dispensing instructions. Also included is a medication calendar strip for tracking daily doses over several weeks.*
FDA Label Image

Package Label-principal Display Panel (40 mg (30 Tablets Bottle))

Package Label-principal Display Panel (40 mg (30 Tablets Bottle))
Label for Citalopram Tablets, USP 40 mg film-coated tablets by Aurobindo Pharma Limited. The label includes dosage strength, quantity of 30 tablets, storage instructions, and distributor information for Aurobindo Pharma USA, Inc. The label is marked Rx only and includes a note to dispense with medication guide separately.*
FDA Label Image

Package Label-principal Display Panel (40 mg Blister Carton (10 x 10 Unit-dose))

Package Label-principal Display Panel (40 mg Blister Carton (10 x 10 Unit-dose))
Packaging label for Citalopram Tablets, USP 40 mg film-coated tablets by Aurobindo Pharma Limited. The label indicates a package of 10 x 10 (100) unit dose tablets and includes dosage strength clearly marked in orange. The label also advises pharmacists to dispense with a separate medication guide.*
FDA Label Image

Package Label-principal Display Panel (40 mg Unit-of-Use Pack (30 Tablets))

Package Label-principal Display Panel (40 mg Unit-of-Use Pack (30 Tablets))
Label for Citalopram Tablets USP 40 mg film-coated tablets by Aurobindo Pharma Limited. The label includes an NDC number 65862-007-32 and states "Rx only." It shows a 30-tablet count and instructions to dispense with a medication guide. The packaging also features a weekly pill reminder layout with days of the week and a push-through blister design for dosage tracking.*
FDA Label Image

Chemical Structure (Citalopram Str)

Chemical Structure (Citalopram Str)
Chemical structure of Citalopram Hydrobromide shown as a two-dimensional molecular diagram depicting its atomic bonds and arrangement.*

* 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.