01 2Chifeng Pharmaceutical Co.,Ltd
02 1DATONG TONGXING ANTIBIOTIC CO., LTD.
03 2Hebei Jianmin Starch Glucose Co., Ltd.
04 2Hebei Shengxue Dacheng Pharmaceutical Company, Ltd.
05 1INNER MONGOLIA HUASHU BIOLOGICAL TECHNOLOGY CO. LTD.
06 1Inner Mongolia Shengxue Dacheng Pharmaceutical Co., Ltd.
07 1JIANGSU TIANHE PHARMACEUTICAL CO LTD
08 1Sichuan Long March Pharmaceutical Co. Ltd.
01 4OXYTETRACYCLINE
02 1OXYTETRACYCLINE DIHYDRATE
03 5Oxytetracycline
04 1Oxytetracycline Dihydrate
01 10China
02 1Blank
NDC Package Code : 54509-0001
Start Marketing Date : 2013-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54509-0003
Start Marketing Date : 2013-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 24507-002
Start Marketing Date : 2019-12-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 24507-001
Start Marketing Date : 2011-01-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70831-101
Start Marketing Date : 2016-07-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60264-110
Start Marketing Date : 2003-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60264-115
Start Marketing Date : 2004-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51671-0002
Start Marketing Date : 2010-12-17
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69169-124
Start Marketing Date : 2024-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 81157-0620
Start Marketing Date : 2016-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Oxytetracycline Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxytetracycline Dihydrate, including repackagers and relabelers. The FDA regulates Oxytetracycline Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxytetracycline Dihydrate 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 Oxytetracycline Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxytetracycline Dihydrate supplier is an individual or a company that provides Oxytetracycline Dihydrate active pharmaceutical ingredient (API) or Oxytetracycline Dihydrate finished formulations upon request. The Oxytetracycline Dihydrate suppliers may include Oxytetracycline Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Oxytetracycline Dihydrate 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 Oxytetracycline Dihydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oxytetracycline Dihydrate 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 Oxytetracycline Dihydrate 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 Oxytetracycline Dihydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oxytetracycline Dihydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oxytetracycline Dihydrate suppliers with NDC on PharmaCompass.
We have 6 companies offering Oxytetracycline Dihydrate
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