01 1PURE AND CURE HEALTHCARE PRIVATE LIMITED
02 1Pfizer Ireland Pharmaceuticals Unlimited Company
03 1Viatris Pharmaceuticals LLC
01 1AZITHROMYCIN, UNSPECIFIED FORM
02 2Azithromycin
01 2U.S.A
02 1Blank
AZITHROMYCIN, UNSPECIFIED FORM
NDC Package Code : 60715-3150
Start Marketing Date : 2011-12-29
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
AZITHROMYCIN, UNSPECIFIED FORM
NDC Package Code : 65427-310
Start Marketing Date : 2014-04-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
AZITHROMYCIN, UNSPECIFIED FORM
NDC Package Code : 82608-001
Start Marketing Date : 2022-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Azithromycin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Azithromycin manufacturer or Azithromycin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Azithromycin manufacturer or Azithromycin supplier.
PharmaCompass also assists you with knowing the Azithromycin API Price utilized in the formulation of products. Azithromycin API Price is not always fixed or binding as the Azithromycin Price is obtained through a variety of data sources. The Azithromycin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ultreon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ultreon, including repackagers and relabelers. The FDA regulates Ultreon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ultreon 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 Ultreon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ultreon supplier is an individual or a company that provides Ultreon active pharmaceutical ingredient (API) or Ultreon finished formulations upon request. The Ultreon suppliers may include Ultreon API manufacturers, exporters, distributors and traders.
click here to find a list of Ultreon 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 Ultreon as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ultreon 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 Ultreon 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 Ultreon and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ultreon NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ultreon suppliers with NDC on PharmaCompass.
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