DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr.Reddy's Laboratories Limited
02 1Assia Chemical Industries Ltd - Teva Tech Site
03 1Emcure Pharmaceuticals Limited
04 1Gador S.A.
05 1Hetero Labs Limited
06 1Maprimed S.A.
07 1Natco Pharma Limited
08 1SHILPA PHARMA LIFESCIENCES LIMITED
09 1ScinoPharm Taiwan Ltd.
10 1USV Private Limited
11 1Yung Shin Pharmaceutical Ind. Co., Ltd.
01 9Zoledronic Acid
02 1Zoledronic acid
03 1Zoledronic acid Monohydrate
01 2Argentina
02 6India
03 1Israel
04 2Taiwan
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-813
Start Marketing Date : 2008-02-18
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63415-0532
Start Marketing Date : 2023-07-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-836
Start Marketing Date : 2022-02-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65797-0006
Start Marketing Date : 2012-04-18
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68554-0037
Start Marketing Date : 1995-12-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57741-2600
Start Marketing Date : 2007-05-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63850-7104
Start Marketing Date : 2016-01-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-1144
Start Marketing Date : 2006-04-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62147-0125
Start Marketing Date : 2010-01-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63126-906
Start Marketing Date : 2012-12-26
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 Zoledronic Acid 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 Zoledronic Acid manufacturer or Zoledronic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zoledronic Acid manufacturer or Zoledronic Acid supplier.
PharmaCompass also assists you with knowing the Zoledronic Acid API Price utilized in the formulation of products. Zoledronic Acid API Price is not always fixed or binding as the Zoledronic Acid Price is obtained through a variety of data sources. The Zoledronic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zometa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zometa, including repackagers and relabelers. The FDA regulates Zometa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zometa 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 Zometa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zometa supplier is an individual or a company that provides Zometa active pharmaceutical ingredient (API) or Zometa finished formulations upon request. The Zometa suppliers may include Zometa API manufacturers, exporters, distributors and traders.
click here to find a list of Zometa 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 Zometa as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Zometa 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 Zometa 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 Zometa and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zometa NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Zometa suppliers with NDC on PharmaCompass.
We have 11 companies offering Zometa
Get in contact with the supplier of your choice:
