DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 2Dr.Reddy's Laboratories Limited
02 1Aurobindo Pharma Limited
03 1Emcure Pharmaceuticals Limited
04 1Natco Pharma Limited
01 3Ibandronate Sodium
02 1Ibandronate sodium form beta
03 1Ibandronate sodium monohydrate
01 5India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-872
Start Marketing Date : 2007-04-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-897
Start Marketing Date : 2008-12-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-270
Start Marketing Date : 2024-01-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-853
Start Marketing Date : 2022-02-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63850-4355
Start Marketing Date : 2016-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Ibandronic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ibandronic Acid, including repackagers and relabelers. The FDA regulates Ibandronic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ibandronic Acid 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 Ibandronic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ibandronic Acid supplier is an individual or a company that provides Ibandronic Acid active pharmaceutical ingredient (API) or Ibandronic Acid finished formulations upon request. The Ibandronic Acid suppliers may include Ibandronic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Ibandronic Acid 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 Ibandronic Acid as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ibandronic Acid 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 Ibandronic Acid 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 Ibandronic Acid and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ibandronic Acid NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ibandronic Acid suppliers with NDC on PharmaCompass.
We have 4 companies offering Ibandronic Acid
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