01 1ANUH PHARMA LIMITED
02 1DARMERICA, LLC
03 1Fagron Inc
04 1Galenova Inc
05 1Jiangsu Lianhuan Pharmaceutical Co.,Ltd.
06 1LETCO MEDICAL, LLC
07 1Medisca Inc.
08 1Nanjing White Whale Pharmaceutical Co., Ltd
09 1Professional Compounding Centers of America
10 2Quimica Sintetica S.A.
11 1Reliable Biopharmaceutical LLC
01 4CHLORAMPHENICOL
02 5Chloramphenicol
03 1Chloramphenicol Hemisuccinate
04 1Chloramphenicol micronized
05 1chloramphenicol
01 1Canada
02 1China
03 1India
04 1Netherlands
05 2Spain
06 4U.S.A
07 1United Kingdom
08 1Blank
NDC Package Code : 64677-0002
Start Marketing Date : 2018-04-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 71052-687
Start Marketing Date : 2021-08-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1000g/1000g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-1419
Start Marketing Date : 2021-10-15
End Marketing Date : 2027-02-28
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-1031
Start Marketing Date : 2009-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0203
Start Marketing Date : 2014-07-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0214
Start Marketing Date : 2021-09-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 53069-0010
Start Marketing Date : 1999-02-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53069-0920
Start Marketing Date : 1999-02-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59605-7806
Start Marketing Date : 2014-01-08
End Marketing Date : 2025-05-18
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 66478-0155
Start Marketing Date : 2013-12-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Anacetin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anacetin, including repackagers and relabelers. The FDA regulates Anacetin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anacetin 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 Anacetin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Anacetin supplier is an individual or a company that provides Anacetin active pharmaceutical ingredient (API) or Anacetin finished formulations upon request. The Anacetin suppliers may include Anacetin API manufacturers, exporters, distributors and traders.
click here to find a list of Anacetin 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 Anacetin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Anacetin 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 Anacetin 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 Anacetin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Anacetin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Anacetin suppliers with NDC on PharmaCompass.
We have 10 companies offering Anacetin
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
