Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
01 1Ofichem BV
02 1Chattem Chemicals, Inc.
03 1W. R. Grace & Co.-Conn.
01 3Methenamine Mandelate
01 1Netherlands
02 2U.S.A
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
NDC Package Code : 62675-1072
Start Marketing Date : 2020-11-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61960-6010
Start Marketing Date : 1999-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22568-1968
Start Marketing Date : 2021-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Methenamine Mandelate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methenamine Mandelate, including repackagers and relabelers. The FDA regulates Methenamine Mandelate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methenamine Mandelate 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 Methenamine Mandelate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methenamine Mandelate supplier is an individual or a company that provides Methenamine Mandelate active pharmaceutical ingredient (API) or Methenamine Mandelate finished formulations upon request. The Methenamine Mandelate suppliers may include Methenamine Mandelate API manufacturers, exporters, distributors and traders.
click here to find a list of Methenamine Mandelate 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 Methenamine Mandelate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Methenamine Mandelate 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 Methenamine Mandelate 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 Methenamine Mandelate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Methenamine Mandelate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Methenamine Mandelate suppliers with NDC on PharmaCompass.
We have 3 companies offering Methenamine Mandelate
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