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01 1Interquim, S.A.

02 2AGC Pharma Chemicals Europe, S.L.U.

03 1AURORE PHARMACEUTICALS PRIVATE LIMITED

04 1Aurobindo Pharma Limited

05 1CTX Lifesciences Pvt. Ltd.

06 1Chromo Laboratories India Private Limited

07 1Cipla Ltd.

08 1DARMERICA, LLC

09 1Divi's Laboratories Limited

10 1Glenmark Life Sciences Limited

11 1Henan Huashang Pharmaceutical Co., Ltd.

12 1Ipca Laboratories Limited

13 1Jubilant Pharmova Limited

14 1MSN Pharmachem Private Limited

15 1MYLAN LABORATORIES LIMITED

16 1Micro Labs Limited

17 1Tianish Laboratories Private Limited

18 1UQUIFA Mexico, S.A. de C.V.

19 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD.

20 1Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.

21 1Zhejiang Huahai Pharmaceutical Co., Ltd.

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PharmaCompass

01

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PharmaVenue
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  • fda
  • EDQM
  • WHO-GMP

Virtual BoothInterquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

TELMISARTAN

NDC Package Code : 64552-4026

Start Marketing Date : 2000-04-04

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Interquim

03

PharmaVenue
Not Confirmed
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TELMISARTAN

NDC Package Code : 53104-7624

Start Marketing Date : 2016-01-01

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (25kg/25kg)

Marketing Category : BULK INGREDIENT

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04

PharmaVenue
Not Confirmed
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PharmaVenue
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TELMISARTAN

NDC Package Code : 42419-035

Start Marketing Date : 2024-10-24

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (25kg/25kg)

Marketing Category : BULK INGREDIENT

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05

PharmaVenue
Not Confirmed
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07

PharmaVenue
Not Confirmed
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PharmaVenue
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TELMISARTAN

NDC Package Code : 42571-278

Start Marketing Date : 2013-09-21

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (10kg/10kg)

Marketing Category : BULK INGREDIENT

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08

PharmaVenue
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10

PharmaVenue
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TELMISARTAN

NDC Package Code : 12666-0010

Start Marketing Date : 2009-12-10

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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Telmisartan Manufacturers

A Telmisartan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Telmisartan, including repackagers and relabelers. The FDA regulates Telmisartan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Telmisartan API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Telmisartan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Telmisartan Suppliers

A Telmisartan supplier is an individual or a company that provides Telmisartan active pharmaceutical ingredient (API) or Telmisartan finished formulations upon request. The Telmisartan suppliers may include Telmisartan API manufacturers, exporters, distributors and traders.

click here to find a list of Telmisartan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Telmisartan NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Telmisartan as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Telmisartan API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Telmisartan as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Telmisartan and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Telmisartan NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Telmisartan suppliers with NDC on PharmaCompass.

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.