China's leading API and intermediate manufacturer, offering CMO/CDMO services and exports to 70+ countries, enhancing global health.
01 1Shandong Chenghui Shuangda Pharmaceutical Co., Ltd.
02 1Shandong Chenghui Shuangda Pharmaceutical Co.,Ltd.
03 1FLOWCHEM PHARMA PRIVATE LIMITED
04 1Medisca Inc.
05 1Professional Compounding Centers of America dba PCCA
06 1R.L.Fine Chem Private Limited
07 1RESONANCE LABORATORIES PRIVATE LIMITED
08 1Spectrum Laboratory Products, Inc.
09 1Syn-Tech Chem. & Pharm. Co., Ltd.
10 1W. R. GRACE & CO.-CONN.
01 3PRAMOXINE HYDROCHLORIDE
02 7Pramoxine Hydrochloride
01 2China
02 3India
03 1Taiwan
04 3U.S.A
05 1United Kingdom
China's leading API and intermediate manufacturer, offering CMO/CDMO services and exports to 70+ countries, enhancing global health.
NDC Package Code : 82481-026
Start Marketing Date : 2022-05-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
China's leading API and intermediate manufacturer, offering CMO/CDMO services and exports to 70+ countries, enhancing global health.
NDC Package Code : 82481-026
Start Marketing Date : 2023-01-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82060-002
Start Marketing Date : 2021-04-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 22568-1076
Start Marketing Date : 2021-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0458
Start Marketing Date : 2014-08-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-1914
Start Marketing Date : 2013-06-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 71554-119
Start Marketing Date : 2020-08-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64908-2050
Start Marketing Date : 2012-05-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-5972
Start Marketing Date : 1993-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54871-0101
Start Marketing Date : 1987-11-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Pramoxine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pramoxine Hydrochloride, including repackagers and relabelers. The FDA regulates Pramoxine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pramoxine Hydrochloride 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 Pramoxine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pramoxine Hydrochloride supplier is an individual or a company that provides Pramoxine Hydrochloride active pharmaceutical ingredient (API) or Pramoxine Hydrochloride finished formulations upon request. The Pramoxine Hydrochloride suppliers may include Pramoxine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Pramoxine Hydrochloride 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 Pramoxine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pramoxine Hydrochloride 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 Pramoxine Hydrochloride 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 Pramoxine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pramoxine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Pramoxine Hydrochloride suppliers with NDC on PharmaCompass.
We have 9 companies offering Pramoxine Hydrochloride
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