Inke S.A: APIs manufacturing plant.
01 1Inke SA
02 1Sicor de Mexico S.A. de C.V
01 1Olodaterol HCl
02 1Olodaterol Hydrochloride
01 1Mexico
02 1Spain
Inke S.A: APIs manufacturing plant.
NDC Package Code : 64567-0031
Start Marketing Date : 2023-07-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63592-7600
Start Marketing Date : 2023-02-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Olodaterol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Olodaterol Hydrochloride, including repackagers and relabelers. The FDA regulates Olodaterol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Olodaterol Hydrochloride 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 Olodaterol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Olodaterol Hydrochloride supplier is an individual or a company that provides Olodaterol Hydrochloride active pharmaceutical ingredient (API) or Olodaterol Hydrochloride finished formulations upon request. The Olodaterol Hydrochloride suppliers may include Olodaterol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Olodaterol Hydrochloride 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 Olodaterol Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Olodaterol Hydrochloride 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 Olodaterol Hydrochloride 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 Olodaterol Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Olodaterol Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Olodaterol Hydrochloride suppliers with NDC on PharmaCompass.
We have 2 companies offering Olodaterol Hydrochloride
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