Citalopram Hydrobromide
Product Images NDC 51655-667

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Citalopram Hydrobromide (NDC 51655-667). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Pharmaceuticals, 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

51655 664 25 Master Bottle Label Approval Rev A 12 20

51655 664 25 Master Bottle Label Approval   Rev A 12 20
This is a description of a package of Citalopram tablets, in 20mg strength, containing 60 tablets, with NDC code 51655-664-25. The package is RX-only and must be stored at 20°-25°C (68°-77°F) with some excursions allowed. The product should be kept away from children and stored in its original container. The manufacturer is Torrent Pharma, Inc. and Lot number is 0000000000; repackaged by Northwind Pharmaceuticals in Indianapolis, IN, with GTIN of 00351655664254. This package is a hydrobromide, USP equivalent to 20mg, and contains citalopram. It was repackaged from 13668-010-05, with S/N: 000000000000000. The expiration date is not readable.*
FDA Label Image

51655 667 52 Master Bottle Label Approval Rev A 01 21

51655 667 52 Master Bottle Label Approval   Rev A 01 21
This is a description of a medication called Citalopram, which comes in the form of 30 tablets, with each tablet containing 40mg of hydrobromide USP. The tablets are manufactured by Torrent Pharma, and the lot number is 0000000000. The medication should be stored in its original container at a temperature range of 20°C-25°C (68°-77°F), with excursions allowed up to 15°C-30°C (59°-86°F) as per USP Controlled Room Temperature. The expiry date for this medication is 00/00/0000. The NDC code for this medication is 51655-667-52 R A 0121, and it is only available through a prescription. The medication should be kept out of the reach of children. The text mentions Northwind Pharmaceuticals as the repackager of the medication.*
FDA Label Image

B35147fd 7d3d 47bc Beca B3a7c3762ed1 01

FDA Label Image

B35147fd 7d3d 47bc Beca B3a7c3762ed1 02

FDA Label Image

B35147fd 7d3d 47bc Beca B3a7c3762ed1 03

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.