DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr.Reddy's Laboratories Limited
02 1Amino Chemicals Ltd
03 1Apotex Inc.
04 1Aurobindo Pharma Limited
05 1Chromo Laboratories India Private Limited
06 1Dr.Reddy┐s Laboratories Limited
07 1Jubilant Biosys limited
08 1LUPIN LIMITED
09 1Pfizer Asia Manufacturing Pte Ltd
10 1Zydus Lifesciences Limited
01 1ZIPRASIDONE HYDROCHLORIDE
02 1Ziprasidone
03 4Ziprasidone Hydrochloride
04 2Ziprasidone Hydrochloride Monohydrate
05 2ziprasidone hydrochloride
01 1Canada
02 6India
03 1Malta
04 1U.S.A
05 1Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
ZIPRASIDONE HYDROCHLORIDE ANHYDROUS
NDC Package Code : 55111-801
Start Marketing Date : 2004-12-23
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66005-0027
Start Marketing Date : 2009-04-29
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49867-0044
Start Marketing Date : 2017-12-29
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-398
Start Marketing Date : 2024-01-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52562-010
Start Marketing Date : 2020-04-09
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65372-1160
Start Marketing Date : 2011-05-24
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57297-330
Start Marketing Date : 2017-03-20
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68724-5235
Start Marketing Date : 2001-02-05
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65841-157
Start Marketing Date : 2018-01-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55111-890
Start Marketing Date : 2007-12-17
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Ziprasidone Hydrochloride 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 Ziprasidone Hydrochloride manufacturer or Ziprasidone Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ziprasidone Hydrochloride manufacturer or Ziprasidone Hydrochloride supplier.
PharmaCompass also assists you with knowing the Ziprasidone Hydrochloride API Price utilized in the formulation of products. Ziprasidone Hydrochloride API Price is not always fixed or binding as the Ziprasidone Hydrochloride Price is obtained through a variety of data sources. The Ziprasidone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Geodon;Zeldox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Geodon;Zeldox, including repackagers and relabelers. The FDA regulates Geodon;Zeldox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Geodon;Zeldox 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 Geodon;Zeldox manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Geodon;Zeldox supplier is an individual or a company that provides Geodon;Zeldox active pharmaceutical ingredient (API) or Geodon;Zeldox finished formulations upon request. The Geodon;Zeldox suppliers may include Geodon;Zeldox API manufacturers, exporters, distributors and traders.
click here to find a list of Geodon;Zeldox 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 Geodon;Zeldox as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Geodon;Zeldox 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 Geodon;Zeldox 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 Geodon;Zeldox and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Geodon;Zeldox NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Geodon;Zeldox suppliers with NDC on PharmaCompass.
We have 9 companies offering Geodon;Zeldox
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