Inke S.A: APIs manufacturing plant.
01 1Inke SA
02 1VAMSI LABS LIMITED.
03 1Wavelength Enterprises LTD
04 1Cerbios-Pharma SA
05 3Industriale Chimica s.r.l.
06 1Lianyungang Runzhong Pharmaceutical Co., Ltd.
01 1TIOTROPIUM BROMIDE MONOHYDRATE
02 2Tiotropium Bromide
03 3Tiotropium Bromide Monohydrate
04 1Tiotropium Bromide Monomethanolate
05 1Tiotropium bromide monohydrate
01 1China
02 1France
03 1India
04 3Italy
05 1Spain
06 1Switzerland
TIOTROPIUM BROMIDE MONOHYDRATE
NDC Package Code : 64567-0026
Start Marketing Date : 2021-01-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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...
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
NDC Package Code : 58175-0565
Start Marketing Date : 2011-12-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
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 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 : 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 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
A Tiotropium Bromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiotropium Bromide, including repackagers and relabelers. The FDA regulates Tiotropium Bromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiotropium Bromide 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 Tiotropium Bromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tiotropium Bromide supplier is an individual or a company that provides Tiotropium Bromide active pharmaceutical ingredient (API) or Tiotropium Bromide finished formulations upon request. The Tiotropium Bromide suppliers may include Tiotropium Bromide API manufacturers, exporters, distributors and traders.
click here to find a list of Tiotropium Bromide 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 Tiotropium Bromide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tiotropium Bromide 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 Tiotropium Bromide 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 Tiotropium Bromide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tiotropium Bromide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tiotropium Bromide suppliers with NDC on PharmaCompass.
We have 6 companies offering Tiotropium Bromide
Get in contact with the supplier of your choice:
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