01 1Boehringer Ingelheim Pharma GmbH and Co. KG
02 1Professional; Compounding Centers of America
01 2BUTYLSCOPOLAMINE BROMIDE
01 1Germany
02 1United Kingdom
NDC Package Code : 12714-011
Start Marketing Date : 2019-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0206
Start Marketing Date : 2000-07-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Scobutyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Scobutyl, including repackagers and relabelers. The FDA regulates Scobutyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Scobutyl 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 Scobutyl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Scobutyl supplier is an individual or a company that provides Scobutyl active pharmaceutical ingredient (API) or Scobutyl finished formulations upon request. The Scobutyl suppliers may include Scobutyl API manufacturers, exporters, distributors and traders.
click here to find a list of Scobutyl 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 Scobutyl as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Scobutyl 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 Scobutyl 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 Scobutyl and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Scobutyl NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Scobutyl suppliers with NDC on PharmaCompass.
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