Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1PolyCarbon Industries, Inc.
02 1Pfanstiehl, Inc.
03 1Analytecon SA
01 2Podofilox
02 1Podophyllotoxin 184
01 1France
02 1Switzerland
03 1U.S.A
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
NDC Package Code : 65571-0022
Start Marketing Date : 2005-10-05
End Marketing Date : 2026-12-21
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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 : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66245-001
Start Marketing Date : 2002-01-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A PODOFILOX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PODOFILOX, including repackagers and relabelers. The FDA regulates PODOFILOX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PODOFILOX 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 PODOFILOX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PODOFILOX supplier is an individual or a company that provides PODOFILOX active pharmaceutical ingredient (API) or PODOFILOX finished formulations upon request. The PODOFILOX suppliers may include PODOFILOX API manufacturers, exporters, distributors and traders.
click here to find a list of PODOFILOX 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 PODOFILOX as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for PODOFILOX 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 PODOFILOX 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 PODOFILOX and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a PODOFILOX NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of PODOFILOX suppliers with NDC on PharmaCompass.
We have 3 companies offering PODOFILOX
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