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01 1Fermion Oy
02 1APICORE PHARMACEUTICALS PRIVATE LIMITED
03 1Azico Biophore India Private Limited
04 1MYLAN LABORATORIES LIMITED
05 1Professional Compounding Centers of America
06 1Professional Compounding Centers of America dba PCCA
07 1Tianish Laboratories Private Limited
01 5NADOLOL
02 1Nadolol
03 1nadolol
01 1Finland
02 3India
03 1U.S.A
04 2United Kingdom
NDC Package Code : 12780-0154
Start Marketing Date : 1986-04-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42973-148
Start Marketing Date : 2008-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69575-4016
Start Marketing Date : 2021-12-16
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-2776
Start Marketing Date : 2013-06-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0238
Start Marketing Date : 2022-05-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 84206-0067
Start Marketing Date : 2024-08-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-718
Start Marketing Date : 2015-01-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Nadolol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nadolol, including repackagers and relabelers. The FDA regulates Nadolol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nadolol 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 Nadolol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nadolol supplier is an individual or a company that provides Nadolol active pharmaceutical ingredient (API) or Nadolol finished formulations upon request. The Nadolol suppliers may include Nadolol API manufacturers, exporters, distributors and traders.
click here to find a list of Nadolol 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 Nadolol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Nadolol 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 Nadolol 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 Nadolol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nadolol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Nadolol suppliers with NDC on PharmaCompass.
We have 6 companies offering Nadolol
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