01 1ACS Dobfar SPA
02 1FUJIAN FUKANG PHARMACEUTICAL CO., LTD
03 1Fagron Inc
04 1Kalchem International inc
05 1LETCO MEDICAL, LLC
06 1Lek Pharmaceuticals, d.d.
07 1Livzon Group Fuzhou Fuxing Pharmaceutical Co., Ltd.
08 1Medisca Inc.
09 2Professional Compounding Centers of America dba PCCA
01 4GENTAMICIN SULFATE
02 1Gentamicin Sulate
03 4Gentamicin Sulfate
04 1Gentamicin sulfate
01 2China
02 1Italy
03 1Netherlands
04 1Slovenia
05 3U.S.A
06 2United Kingdom
NDC Package Code : 52946-0605
Start Marketing Date : 2010-04-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0775
Start Marketing Date : 1998-04-01
End Marketing Date : 2026-03-03
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 67630-0003
Start Marketing Date : 2011-03-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60592-301
Start Marketing Date : 2019-11-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 48866-8256
Start Marketing Date : 2013-07-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 62991-1072
Start Marketing Date : 2011-03-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 42513-0008
Start Marketing Date : 2014-09-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0632
Start Marketing Date : 2014-06-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0252
Start Marketing Date : 2020-08-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1610
Start Marketing Date : 2013-06-28
End Marketing Date : 2025-07-26
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Gentamicin Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gentamicin Sulfate, including repackagers and relabelers. The FDA regulates Gentamicin Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gentamicin Sulfate 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 Gentamicin Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gentamicin Sulfate supplier is an individual or a company that provides Gentamicin Sulfate active pharmaceutical ingredient (API) or Gentamicin Sulfate finished formulations upon request. The Gentamicin Sulfate suppliers may include Gentamicin Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Gentamicin Sulfate 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 Gentamicin Sulfate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Gentamicin Sulfate 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 Gentamicin Sulfate 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 Gentamicin Sulfate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Gentamicin Sulfate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Gentamicin Sulfate suppliers with NDC on PharmaCompass.
We have 9 companies offering Gentamicin Sulfate
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