Metoprolol Tartrate Tablet
Product Images NDC 52817-252

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Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate (NDC 52817-252). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Trupharma 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

Metoprolol Tartrate Tablets, Usp 100 mg (NDC 52817-254-10)

Metoprolol Tartrate Tablets, Usp 100 mg (NDC 52817-254-10)
This text provides information about a medication containing 100 mg of Metoprolol tartrate. The recommended dosage and storage instructions are included, such as keeping it in a tightly closed container away from moisture and at controlled room temperature. The medication is available in a pack of 100 tablets and is distributed by TruPharma, LLC in Tampa, FL, with manufacturing done by Rubicon Research Ltd. in Thane, India. The NDC code and manufacturing information are also provided.*
FDA Label Image

Metoprolol Tartrate Tablets, Usp 100 mg (NDC 52817-254-00)

Metoprolol Tartrate Tablets, Usp 100 mg (NDC 52817-254-00)
This is a product description for Metoprolol tartrate tablets, each containing 100 mg of the active ingredient. The usual dosage information is provided in the package insert. The tablets should be stored in a tightly closed, light-resistant container at temperatures between 20°C to 25°C, protected from moisture and kept out of reach of children. The product is distributed by TruPharma, LLC in Tampa, FL, and manufactured by Rubicon Research Ltd. in Thane, India. The package contains 1,000 tablets and is for prescription use only.*
FDA Label Image

Metoprolol Tartrate Tablets, Usp 25 mg (NDC 52817-250-10)

Metoprolol Tartrate Tablets, Usp 25 mg (NDC 52817-250-10)
This text provides information about Metoprolol tartrate tablets, with each uncoated tablet containing 25 mg of the active pharmaceutical ingredient. The recommended dosage and storage instructions are also included, emphasizing the need for a tight, light-resistant container with a child-resistant closure. The manufacturer and distributor details are given along with the NDC code for identification. Keep the medication away from children, store it at 20°C to 25°C, and protect it from moisture.*
FDA Label Image

Metoprolol Tartrate Tablets, Usp 25 mg (NDC 52817-250-00)

Metoprolol Tartrate Tablets, Usp 25 mg (NDC 52817-250-00)
This text provides information about Metoprolol Tartrate tablets, each containing 25 mg of the active ingredient. It includes details on the recommended dosage, storage conditions (between 20°C to 25°C), protection from moisture, and the importance of keeping the medication out of the reach of children. The manufacturer and distributor details are also mentioned, along with the NDC number for identification purposes.*
FDA Label Image

Metoprolol Tartrate Tablets, Usp 37.5 mg (NDC 52817-251-10)

Metoprolol Tartrate Tablets, Usp 37.5 mg (NDC 52817-251-10)
This product is Metoprolol tartrate tablets, each containing 37.5 mg of the active ingredient. The usual dosage can be found in the package insert. It is essential that these tablets are stored in a tight, light-resistant container with a child-resistant closure at temperatures between 20°C to 25°C (68°F to 77°F) to protect them from moisture. The packaging also includes the National Drug Code (NDC) for identification. This medication should be kept out of reach of children. The tablets are manufactured by Rubicon Research Ltd. in Thane, India, and distributed by TruPharma, LLC in Tampa, Florida. The package contains 100 tablets and is for prescription use only.*
FDA Label Image

Metoprolol Tartrate Tablets, Usp 50 mg (NDC 52817-252-10)

Metoprolol Tartrate Tablets, Usp 50 mg (NDC 52817-252-10)
The text includes information about Metoprolol tartrate 50 mg tablets. The usual dosage information is available in the package insert. It emphasizes the need to store the medication in a tightly closed, light-resistant, and child-resistant container at a temperature between 20°C to 25°C. The manufacturer is Rubicon Research Ltd. from Thane, India, and the product is distributed by TruPharma, LLC in Tampa, FL. The NDC code for the tablets is 52817-252-10.*
FDA Label Image

Metoprolol Tartrate Tablets, Usp 50 mg (NDC 52817-252-00)

Metoprolol Tartrate Tablets, Usp 50 mg (NDC 52817-252-00)
This is a medical product containing Metoprolol tartrate, USP in a 50 mg dosage. It is distributed by TruPharma, LLC in Tampa, FL. The usual dosage can be found in the package insert. The tablets are manufactured by Rubicon Research Ltd. in Thane, India. It is important to dispense and store the tablets in a light-resistant container with a child-resistant closure at a temperature between 20°C to 25°C (68°F to 77°F). Keep the medication out of the reach of children and protect from moisture.*
FDA Label Image

Metoprolol Tartrate Tablets, Usp 75 mg (NDC 52817-253-10)

Metoprolol Tartrate Tablets, Usp 75 mg (NDC 52817-253-10)
This information pertains to an uncoated tablet containing 75 mg of Metoprolol tartrate. The product is distributed by TruPharma, LLC and manufactured by Rubicon Research Ltd. The usual dosage instructions are provided in the package insert. It is recommended to dispense in a tight, light-resistant container using a child-resistant closure. The medication should be stored at a temperature between 20°C to 25°C and protected from moisture. The container should be kept tightly closed and out of reach of children.*
FDA Label Image

Metoprolol Tartrate Tablet Structure (Metoprolol Tartrate Tabs Structure)

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