01 1Hebei Jianmin Starch Glucose Co., Ltd.
02 1Hebei Shengxue Dacheng Pharmaceutical Co., Ltd.
03 1Hebei Shengxue Dacheng Pharmaceutical Company, Ltd.
04 1Inner Mongolia Shengxue Dacheng Pharmaceutical Co., Ltd.
05 1Jiangsu Tianhe Pharmaceutical Co., Ltd.
06 1Sichuan Long March Pharmaceutical Co. Ltd.
07 2YANGZHOU LIBERTY PHARMACEUTICAL CO. LTD
01 1OXYTETRACYCLINE DIHYDRATE
02 1OXYTETRACYCLINE HCL
03 3OXYTETRACYCLINE HYDROCHLORIDE
04 1OXYTETRACYCLINE HYDROCHLORIDE MICRONIZED
05 2Oxytetracycline Hydrochloride
01 8China
NDC Package Code : 54509-0002
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 : 24507-003
Start Marketing Date : 2015-01-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 24507-004
Start Marketing Date : 2022-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82403-002
Start Marketing Date : 2022-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51671-0003
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 : 69169-116
Start Marketing Date : 2020-09-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71057-0100
Start Marketing Date : 2016-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71057-0200
Start Marketing Date : 2016-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Oxytetracycline Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxytetracycline Hydrochloride, including repackagers and relabelers. The FDA regulates Oxytetracycline Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxytetracycline Hydrochloride 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 Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxytetracycline Hydrochloride supplier is an individual or a company that provides Oxytetracycline Hydrochloride active pharmaceutical ingredient (API) or Oxytetracycline Hydrochloride finished formulations upon request. The Oxytetracycline Hydrochloride suppliers may include Oxytetracycline Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Oxytetracycline Hydrochloride 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 Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oxytetracycline Hydrochloride 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 Hydrochloride 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 Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oxytetracycline Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oxytetracycline Hydrochloride suppliers with NDC on PharmaCompass.
We have 5 companies offering Oxytetracycline Hydrochloride
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