Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
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01 1VAMSI LABS LIMITED.
02 1Boehringer Ingelheim Pharma GmbH and Co. KG
03 1Cerbios-Pharma SA
04 3Industriale Chimica s.r.l.
05 1Lianyungang Runzhong Pharmaceutical Co., Ltd.
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01 1Tiotropium Bromide
02 3Tiotropium Bromide Monohydrate
03 1Tiotropium Bromide Monomethanolate
04 1Tiotropium bromide monohydrate
05 1tiotropium bromide
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01 1China
02 1Germany
03 1India
04 3Italy
05 1Switzerland
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
TIOTROPIUM BROMIDE MONOHYDRATE
NDC Package Code : 66412-0761
Start Marketing Date : 2020-04-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 12714-915
Start Marketing Date : 2015-05-21
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54239-011
Start Marketing Date : 2014-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
TIOTROPIUM BROMIDE MONOHYDRATE
NDC Package Code : 63190-0560
Start Marketing Date : 2004-01-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
TIOTROPIUM BROMIDE MONOMETHANOLATE
NDC Package Code : 63190-0640
Start Marketing Date : 2004-01-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
TIOTROPIUM BROMIDE MONOHYDRATE
NDC Package Code : 63190-0380
Start Marketing Date : 2011-07-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
TIOTROPIUM BROMIDE MONOHYDRATE
NDC Package Code : 61662-0021
Start Marketing Date : 2023-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Tiotropium Bromide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Tiotropium Bromide manufacturer or Tiotropium Bromide supplier for your needs.
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A Respimat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Respimat, including repackagers and relabelers. The FDA regulates Respimat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Respimat 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 Respimat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Respimat supplier is an individual or a company that provides Respimat active pharmaceutical ingredient (API) or Respimat finished formulations upon request. The Respimat suppliers may include Respimat API manufacturers, exporters, distributors and traders.
click here to find a list of Respimat 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 Respimat as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Respimat 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 Respimat 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 Respimat and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Respimat NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Respimat suppliers with NDC on PharmaCompass.
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