Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
01 1Interquim, S.A.
02 1Dr.Reddy's Laboratories Limited
03 1Pharmacia & Upjohn Company LLC
04 1Aurobindo Pharma Limited
05 1Cipla Ltd.
06 1Emcure Pharmaceuticals Limited
07 1Erregierre SpA
08 1Hetero Drugs Limited
09 1MSN Pharmachem Private Limited
10 1Maithri Laboratories Private Limited
11 1UQUIFA Mexico, S.A. DE C.V.
12 1Unichem Laboratories Limited, India
13 2Viatris Pharmaceuticals LLC
01 12Tolterodine Tartrate
02 1Tolterodine tartrate
03 1tolterodine
01 8India
02 1Italy
03 2Spain
04 3U.S.A
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
NDC Package Code : 64552-4002
Start Marketing Date : 2000-12-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-855
Start Marketing Date : 2004-10-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
NDC Package Code : 0009-0420
Start Marketing Date : 2014-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7572
Start Marketing Date : 2016-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-901
Start Marketing Date : 2021-07-21
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49706-1835
Start Marketing Date : 2010-01-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50370-0023
Start Marketing Date : 2010-04-20
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-035
Start Marketing Date : 2011-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52286-0018
Start Marketing Date : 2009-11-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65427-020
Start Marketing Date : 2014-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Tolterodine Tartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tolterodine Tartrate, including repackagers and relabelers. The FDA regulates Tolterodine Tartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tolterodine Tartrate 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 Tolterodine Tartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tolterodine Tartrate supplier is an individual or a company that provides Tolterodine Tartrate active pharmaceutical ingredient (API) or Tolterodine Tartrate finished formulations upon request. The Tolterodine Tartrate suppliers may include Tolterodine Tartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Tolterodine Tartrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Tolterodine Tartrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tolterodine Tartrate API and other APIs are published in this directory by the FDA.
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 Tolterodine Tartrate 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.
The NDC directory also contains data on finished compounded human drug products that contain Tolterodine Tartrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tolterodine Tartrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tolterodine Tartrate suppliers with NDC on PharmaCompass.
We have 12 companies offering Tolterodine Tartrate
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