Veranova: A CDMO that manages complexity with confidence.
01 1Veranova, L.P.
02 1Noramco, LLC
03 1Chattem Chemicals, Inc.
04 1Medisca Inc.
05 1Professional Compounding Centers of America
06 1Professional Compounding Centers of America dba PCCA
07 1Siegfried USA, LLC
08 3SpecGx LLC
01 3CODEINE PHOSPHATE
02 6Codeine Phosphate
03 1Codeine Phosphate Hemihydrate
01 3Ireland
02 1Switzerland
03 4U.S.A
04 2United Kingdom
NDC Package Code : 49812-0051
Start Marketing Date : 2019-09-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
NDC Package Code : 51634-0999
Start Marketing Date : 1986-06-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61960-0380
Start Marketing Date : 2019-10-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-1561
Start Marketing Date : 1975-08-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-1548
Start Marketing Date : 1973-06-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-1550
Start Marketing Date : 1986-12-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0679
Start Marketing Date : 2014-08-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0335
Start Marketing Date : 2024-04-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1013
Start Marketing Date : 2002-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0792-0644
Start Marketing Date : 2007-01-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Codeine Phosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Codeine Phosphate, including repackagers and relabelers. The FDA regulates Codeine Phosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Codeine Phosphate 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 Codeine Phosphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Codeine Phosphate supplier is an individual or a company that provides Codeine Phosphate active pharmaceutical ingredient (API) or Codeine Phosphate finished formulations upon request. The Codeine Phosphate suppliers may include Codeine Phosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Codeine Phosphate 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 Codeine Phosphate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Codeine Phosphate 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 Codeine Phosphate 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 Codeine Phosphate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Codeine Phosphate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Codeine Phosphate suppliers with NDC on PharmaCompass.
We have 7 companies offering Codeine Phosphate
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