Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 4Pharmaceutical Works POLPHARMA
02 1Amoli Organics (A Division of Umedica Laboratories Pvt.Ltd.)
03 1Aurobindo Pharma Limited
04 1CTX Lifesciences Pvt. Ltd.
05 1Cambrex Profarmaco Milano Srl
06 1Changzhou Pharmaceutical Factory
07 3Ipca Laboratories Limited
08 1Professional Compounding Centers of America
09 1Professional Compounding Centers of America dba PCCA
10 1Spectrum Laboratory Products, Inc.
11 1TAPI Croatia Industries Ltd.
12 2Unichem Laboratories Limited, India
13 1Zydus Lifesciences Limited
01 3HYDROCHLOROTHIAZIDE
02 1Hydrchlorothiazide
03 14Hydrochlorothiazide
04 1Hydrochlorothiazide Process 2
01 1China
02 9India
03 4Poland
04 2U.S.A
05 2United Kingdom
06 1Blank
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0405
Start Marketing Date : 1982-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0544
Start Marketing Date : 1982-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (30kg/30kg)
Marketing Category : BULK INGREDIENT
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0605
Start Marketing Date : 1982-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0613
Start Marketing Date : 1982-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12828-0008
Start Marketing Date : 1986-01-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42419-001
Start Marketing Date : 2007-11-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0172
Start Marketing Date : 2011-05-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1611
Start Marketing Date : 2002-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-3575
Start Marketing Date : 1992-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 11722-060
Start Marketing Date : 2015-12-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
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A METHYLDOPA AND HYDROCHLOROTHIAZIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of METHYLDOPA AND HYDROCHLOROTHIAZIDE, including repackagers and relabelers. The FDA regulates METHYLDOPA AND HYDROCHLOROTHIAZIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. METHYLDOPA AND HYDROCHLOROTHIAZIDE 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 METHYLDOPA AND HYDROCHLOROTHIAZIDE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A METHYLDOPA AND HYDROCHLOROTHIAZIDE supplier is an individual or a company that provides METHYLDOPA AND HYDROCHLOROTHIAZIDE active pharmaceutical ingredient (API) or METHYLDOPA AND HYDROCHLOROTHIAZIDE finished formulations upon request. The METHYLDOPA AND HYDROCHLOROTHIAZIDE suppliers may include METHYLDOPA AND HYDROCHLOROTHIAZIDE API manufacturers, exporters, distributors and traders.
click here to find a list of METHYLDOPA AND HYDROCHLOROTHIAZIDE 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 METHYLDOPA AND HYDROCHLOROTHIAZIDE as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for METHYLDOPA AND HYDROCHLOROTHIAZIDE 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 METHYLDOPA AND HYDROCHLOROTHIAZIDE 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 METHYLDOPA AND HYDROCHLOROTHIAZIDE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a METHYLDOPA AND HYDROCHLOROTHIAZIDE NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of METHYLDOPA AND HYDROCHLOROTHIAZIDE suppliers with NDC on PharmaCompass.
We have 11 companies offering METHYLDOPA AND HYDROCHLOROTHIAZIDE
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