01 1Amoli Organics (A Division of Umedica Laboratories Pvt.Ltd.)
02 1CTX Lifesciences Pvt. Ltd.
03 1Chromo Laboratories India Private Limited
04 3Curia Italy S.r.l.
05 1Honour Lab Limited
06 1Ipca Laboratories Limited
07 1MSN Life Sciences Private Limited
08 1Maithri Drugs Private Limited
09 1Unichem Laboratories Limited, India
01 3CHLORTHALIDONE
02 6Chlorthalidone
03 1Chorthalidone
04 1chlorthalidone
01 8India
02 3U.S.A
NDC Package Code : 62512-0026
Start Marketing Date : 1988-07-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52562-003
Start Marketing Date : 2018-08-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42419-032
Start Marketing Date : 2024-10-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 44657-0034
Start Marketing Date : 2012-03-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 44657-0057
Start Marketing Date : 2012-03-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 44657-0058
Start Marketing Date : 2012-03-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69037-0056
Start Marketing Date : 1982-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1134
Start Marketing Date : 2013-10-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70600-008
Start Marketing Date : 2017-11-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-063
Start Marketing Date : 2018-04-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Chlorthalidone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorthalidone, including repackagers and relabelers. The FDA regulates Chlorthalidone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorthalidone 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 Chlorthalidone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorthalidone supplier is an individual or a company that provides Chlorthalidone active pharmaceutical ingredient (API) or Chlorthalidone finished formulations upon request. The Chlorthalidone suppliers may include Chlorthalidone API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorthalidone 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 Chlorthalidone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Chlorthalidone 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 Chlorthalidone 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 Chlorthalidone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Chlorthalidone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Chlorthalidone suppliers with NDC on PharmaCompass.
We have 8 companies offering Chlorthalidone
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