01 1Chemische Fabrik Berg GmbH
02 1COSMA Spa
03 1Calyx Chemicals & Pharmaceuticals
04 1Emcure Pharmaceuticals Limited
05 1Fagron Inc
06 1Fagron Services B.V.
07 1Glochem Industries Private Limited
08 2Ipca Laboratories Limited
09 1Kreative Organics Private Limited
10 1LETCO MEDICAL, LLC
11 1Medisca Inc.
12 1Professional Compounding Centers of America
13 1Spectrum Laboratory Products, Inc.
14 1Srikem Laboratories Pvt. Ltd.
15 2Symed Labs Limited
16 6Vijayasri Organics Private Limited
01 1HYDROXYZINE HYDROCHLORIDE
02 1Hydroxyzine HCl
03 1Hydroxyzine Hcl
04 17Hydroxyzine Hydrochloride
05 2Hydroxyzine hydrochloride
06 1Hydroyxzine Hydrochloride
01 1Germany
02 15India
03 1Italy
04 2Netherlands
05 3U.S.A
06 1United Kingdom
NDC Package Code : 65319-1096
Start Marketing Date : 2019-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51604-0003
Start Marketing Date : 2009-10-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-950
Start Marketing Date : 2023-08-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0485
Start Marketing Date : 2020-06-18
End Marketing Date : 2027-09-30
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 24234-0015
Start Marketing Date : 2023-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1184
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 : 38779-0298
Start Marketing Date : 2014-07-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0272
Start Marketing Date : 2013-06-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-3652
Start Marketing Date : 1989-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 13746-103
Start Marketing Date : 2011-05-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Hydroxyzine Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydroxyzine Dihydrochloride, including repackagers and relabelers. The FDA regulates Hydroxyzine Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydroxyzine Dihydrochloride 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 Hydroxyzine Dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydroxyzine Dihydrochloride supplier is an individual or a company that provides Hydroxyzine Dihydrochloride active pharmaceutical ingredient (API) or Hydroxyzine Dihydrochloride finished formulations upon request. The Hydroxyzine Dihydrochloride suppliers may include Hydroxyzine Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Hydroxyzine Dihydrochloride 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 Hydroxyzine Dihydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Hydroxyzine Dihydrochloride 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 Hydroxyzine Dihydrochloride 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 Hydroxyzine Dihydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Hydroxyzine Dihydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Hydroxyzine Dihydrochloride suppliers with NDC on PharmaCompass.
We have 15 companies offering Hydroxyzine Dihydrochloride
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
