Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.
01 1Pfanstiehl, Inc.
02 1Analytecon SA
01 2Podofilox
01 1Switzerland
02 1U.S.A
Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.
NDC Package Code : 67430-100
Start Marketing Date : 2017-01-23
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66245-001
Start Marketing Date : 2002-01-29
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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A Warticon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Warticon, including repackagers and relabelers. The FDA regulates Warticon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Warticon API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Warticon supplier is an individual or a company that provides Warticon active pharmaceutical ingredient (API) or Warticon finished formulations upon request. The Warticon suppliers may include Warticon API manufacturers, exporters, distributors and traders.
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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 Warticon as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Warticon 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 Warticon 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.
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