01 1Aurobindo Pharma Limited
02 1Covalent Laboratories Private Limited
03 1PURE AND CURE HEALTHCARE PRIVATE LIMITED
01 1CEFIXIME
02 2Cefixime
01 2India
02 1Blank
NDC Package Code : 65862-791
Start Marketing Date : 2023-11-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61788-3000
Start Marketing Date : 2015-04-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82608-007
Start Marketing Date : 2022-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Oroken manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oroken, including repackagers and relabelers. The FDA regulates Oroken manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oroken 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 Oroken manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oroken supplier is an individual or a company that provides Oroken active pharmaceutical ingredient (API) or Oroken finished formulations upon request. The Oroken suppliers may include Oroken API manufacturers, exporters, distributors and traders.
click here to find a list of Oroken 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 Oroken as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oroken 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 Oroken 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 Oroken and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oroken NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oroken suppliers with NDC on PharmaCompass.
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