Trazodone Hydrochloride Tablet
Product Images NDC 64980-673

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Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Trazodone Hydrochloride (NDC 64980-673). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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100mg-score (C52e79ca D40f 4dbc A924 9a4139addd22 04)

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150mg-tablet (C52e79ca D40f 4dbc A924 9a4139addd22 05)

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100mg-break (C52e79ca D40f 4dbc A924 9a4139addd22 06)

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150mg-break (C52e79ca D40f 4dbc A924 9a4139addd22 07)

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200mg-break (C52e79ca D40f 4dbc A924 9a4139addd22 08)

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300mg-break (C52e79ca D40f 4dbc A924 9a4139addd22 09)

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This text provides information about Tramadol Hydrochloride tablets, which contain 50 mg of tramadol hydrochloride USP. It includes instructions for storage, dosage, and dispensing with a child-resistant closure in a light-resistant container. The medication guide can be found online, and the tablets should be kept out of reach of children. The product is manufactured in India and distributed by Rising Pharma Holdings in the United States. The expiration date is September 2024.*
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This is a description of Trazodone Hydrochloride Tablets, USP, containing 100 mg of trazodone hydrochloride USP per tablet. The medication guide should be provided to each patient separately. The tablets should be stored at 20°C to 25°C (68°F to 77°F) with excursions permitted from 15°C to 30°C (59°F to 86°F). Dispense with a child-resistant closure in a tight, light-resistant container. Instructions for usual dosage can be found in the package insert. It is important to keep this medication out of the reach of children. The medication was issued in September 2024 and distributed by Rising Pharma Holdings, Inc. Additional guidance can be found in the Medication Guide available at the provided link.*
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This is a description of Trazodone Hydrochloride Tablets, USP. Each tablet contains 150 mg of Trazodone Hydrochloride USP. The medication guide provided separately should be dispensed to each patient. Store the tablets at 20°C to 25°C with permitted excursions between 15°C to 30°C. The prescription includes instructions for dispensing with a child-resistant closure in a tight, light-resistant container. The pharmacist should instruct the patient on the correct way to break the tablet if not taking a whole one. The usual dosage information is available in the package insert. The medication guide is available online at https:/risingpharma.com/Medguides/Trazodone.pdf. The tablets are manufactured by Graviti Pharmaceuticals Pvt. Ltd. in India and distributed by Rising Pharma Holdings, Inc. in East Brunswick, NJ. The prescription details include an issued date of 09/2024.*
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This text is a detailed medication label for Trazodone Hydrochloride Tablets. It includes information on the dosage, storage conditions, manufacturing details, and safety precautions. It also instructs the pharmacist on how to dispense and advise patients on using the medication correctly. The medication guide is provided separately to each patient.*

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