Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
01 1Laboratorium Ofichem BV
02 1Andhra Organics Limited
03 1Hunan Xiangyikang Pharmaceutical Co., Ltd.
04 1Kalchem International inc
05 1Medisca Inc
06 2Medisca Inc.
07 2VALENS MOLECULES PRIVATE LIMITED
08 2Wugan Pharmaceutical (Suzhou) Co., Ltd.
01 3SULFADIAZINE
02 1SULFADIAZINE SODIUM
03 3Sulfadiazine
04 4Sulfadiazine Sodium
01 3China
02 3India
03 1Netherlands
04 4U.S.A
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
NDC Package Code : 62675-0320
Start Marketing Date : 2018-07-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72672-003
Start Marketing Date : 2023-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71236-0003
Start Marketing Date : 2017-02-15
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 86129-0001
Start Marketing Date : 2020-08-26
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60592-707
Start Marketing Date : 2019-12-13
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-3228
Start Marketing Date : 2021-07-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-3224
Start Marketing Date : 2022-10-18
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0705
Start Marketing Date : 2012-04-16
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62705-0229
Start Marketing Date : 2023-04-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62705-0230
Start Marketing Date : 2023-04-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Sulfadiazine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Sulfadiazine manufacturer or Sulfadiazine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sulfadiazine manufacturer or Sulfadiazine supplier.
A Sulfadiazin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulfadiazin, including repackagers and relabelers. The FDA regulates Sulfadiazin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulfadiazin 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 Sulfadiazin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Sulfadiazin supplier is an individual or a company that provides Sulfadiazin active pharmaceutical ingredient (API) or Sulfadiazin finished formulations upon request. The Sulfadiazin suppliers may include Sulfadiazin API manufacturers, exporters, distributors and traders.
click here to find a list of Sulfadiazin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Sulfadiazin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sulfadiazin 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 Sulfadiazin 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 Sulfadiazin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sulfadiazin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sulfadiazin suppliers with NDC on PharmaCompass.
We have 7 companies offering Sulfadiazin
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