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Navana Pharmaceuticals (DHA:NAVANAPHAR) Total Long-Term Assets : BDT0.00 Mil (As of . 20)


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What is Navana Pharmaceuticals Total Long-Term Assets?

Total Long-Term Assets includes Investments And Advances, Intangible Assets, Property, Plant and Equipment and Other Long Term Assets. Navana Pharmaceuticals's Total Long-Term Assets for the quarter that ended in . 20 was BDT0.00 Mil.

Navana Pharmaceuticals Total Long-Term Assets Historical Data

The historical data trend for Navana Pharmaceuticals's Total Long-Term Assets can be seen below:

* For Operating Data section: All numbers are indicated by the unit behind each term and all currency related amount are in USD.
* For other sections: All numbers are in millions except for per share data, ratio, and percentage. All currency related amount are indicated in the company's associated stock exchange currency.

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Navana Pharmaceuticals Total Long-Term Assets Chart

Navana Pharmaceuticals Annual Data
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Navana Pharmaceuticals Semi-Annual Data
Total Long-Term Assets

Navana Pharmaceuticals Total Long-Term Assets Calculation

Total Long-Term Assets are the sum of the carrying amounts of all assets that are expected to be realized in cash, sold or consumed longer than one year. It includes Investments And Advances, Intangible Assets, Property, Plant and Equipment and Other Long Term Assets.

Navana Pharmaceuticals Total Long-Term Assets Related Terms

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Navana Pharmaceuticals Business Description

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GURUFOCUS.COM » STOCK LIST » Healthcare » Drug Manufacturers » Navana Pharmaceuticals PLC (DHA:NAVANAPHAR) » Definitions » Total Long-Term Assets
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Traded in Other Exchanges
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Address
Road 4, House 99, Block B, Banani, Dhaka, BGD, 1213
Website
https://www.navanapharma.com
Navana Pharmaceuticals PLC operates its business under two divisions namely Veterinary Division and Human Health Division. Veterinary Division manufactures and markets high-quality veterinary medicine and feed supplements for different segments including poultry, dairy and aqua products. Human Health Division operates its manufacturing facilities in strict compliance with WHO cGMP guidelines for the production of tablets, capsules, oral liquids, ampoules, dry powder vials, powder for suspension, eye drops, creams and ointments.

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