Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1NURAY CHEMICALS PRIVATE LIMITED
02 1Neuland Laboratories Limited
03 1Anthem Biosciences Pvt Ltd
04 1Apicore US LLC
05 1Apothecon Pharmaceuticals Pvt Ltd
06 1Aurobindo Pharma Limited
07 1Catalent Micron Technologies, Inc.
08 1DARMERICA, LLC
09 1Professional Compounding Centers of America
10 1Raks Pharma Pvt. Limited
11 1Zhejiang ChemPacific Corporation
01 3PHENOXYBENZAMINE HYDROCHLORIDE
02 1Phenoxybenzamine
03 1Phenoxybenzamine HCl
04 5Phenoxybenzamine Hydrochloride
05 1phenoxybenzamine hydrochloride
01 7India
02 3U.S.A
03 1United Kingdom
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
PHENOXYBENZAMINE HYDROCHLORIDE
NDC Package Code : 58159-044
Start Marketing Date : 2022-10-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Neuland Laboratories- A dedicated 100% API provider.
PHENOXYBENZAMINE HYDROCHLORIDE
NDC Package Code : 58032-1014
Start Marketing Date : 2013-11-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
PHENOXYBENZAMINE HYDROCHLORIDE
NDC Package Code : 14096-114
Start Marketing Date : 2011-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
PHENOXYBENZAMINE HYDROCHLORIDE
NDC Package Code : 76339-143
Start Marketing Date : 2019-09-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (4.999kg/4.999kg)
Marketing Category : BULK INGREDIENT
PHENOXYBENZAMINE HYDROCHLORIDE
NDC Package Code : 59651-298
Start Marketing Date : 2024-01-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
PHENOXYBENZAMINE HYDROCHLORIDE
NDC Package Code : 69988-0016
Start Marketing Date : 2011-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/1)
Marketing Category : DRUG FOR FURTHER PROCESSING
PHENOXYBENZAMINE HYDROCHLORIDE
NDC Package Code : 59981-023
Start Marketing Date : 2011-08-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
PHENOXYBENZAMINE HYDROCHLORIDE
NDC Package Code : 71052-209
Start Marketing Date : 2021-02-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
PHENOXYBENZAMINE HYDROCHLORIDE
NDC Package Code : 51927-0261
Start Marketing Date : 2022-11-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
PHENOXYBENZAMINE HYDROCHLORIDE
NDC Package Code : 47621-309
Start Marketing Date : 2019-09-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Dibenzyline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dibenzyline, including repackagers and relabelers. The FDA regulates Dibenzyline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dibenzyline 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 Dibenzyline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dibenzyline supplier is an individual or a company that provides Dibenzyline active pharmaceutical ingredient (API) or Dibenzyline finished formulations upon request. The Dibenzyline suppliers may include Dibenzyline API manufacturers, exporters, distributors and traders.
click here to find a list of Dibenzyline 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 Dibenzyline as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Dibenzyline 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 Dibenzyline 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 Dibenzyline and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dibenzyline NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Dibenzyline suppliers with NDC on PharmaCompass.
We have 11 companies offering Dibenzyline
Get in contact with the supplier of your choice:
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