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01 1CIPAN-Companhia Industrial Produtora de Antibióticos, S.A.
02 1AX Pharmaceutical Corp
03 1FUJIAN FUKANG PHARMACEUTICAL CO., LTD.
04 1Fagron Inc
05 1LETCO MEDICAL, LLC
06 1Medisca Inc.
07 1Ningxia Qiyuan Pharmaceutical Co., Ltd.
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01 1TETRACYCLINE HYDROCHLORIDE
02 1Tetracycline HCl
03 5Tetracycline Hydrochloride
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01 1Canada
02 2China
03 1Netherlands
04 1Spain
05 2U.S.A
NDC Package Code : 17158-0100
Start Marketing Date : 2017-12-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 73377-301
Start Marketing Date : 2024-11-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51552-0463
Start Marketing Date : 2004-09-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 67630-0007
Start Marketing Date : 2018-09-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-2941
Start Marketing Date : 2010-09-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0053
Start Marketing Date : 2012-02-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59566-0350
Start Marketing Date : 2004-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Actisite manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Actisite, including repackagers and relabelers. The FDA regulates Actisite manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Actisite 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 Actisite manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Actisite supplier is an individual or a company that provides Actisite active pharmaceutical ingredient (API) or Actisite finished formulations upon request. The Actisite suppliers may include Actisite API manufacturers, exporters, distributors and traders.
click here to find a list of Actisite 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 Actisite as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Actisite 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 Actisite 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 Actisite and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Actisite NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Actisite suppliers with NDC on PharmaCompass.
We have 7 companies offering Actisite
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