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List of NDC API details of Levocetirizine Active Pharmaceutical Ingredient listed on PharmaCompass.com

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SERVICES
Flag India
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LEVOCETIRIZINE DIHYDROCHLORIDE
POWDER (25kg/25kg)
BULK INGREDIENT
42765-008
2020-03-18
2024-12-31
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Levocetirizine Dihydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
55111-045
2013-10-09
2024-12-31
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URL Supplier Web Content
LEVOCETIRIZINE DIHYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT
52562-300
2011-09-21
2024-12-31
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Levocetirizine Dihydrochloride-USP
POWDER (1kg/kg)
BULK INGREDIENT
52562-006
2021-12-01
2024-12-31
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Levocetirizine Dihydrochloride
POWDER (25kg/25kg)
BULK INGREDIENT
53104-7644
2016-01-01
2024-12-31
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Levocetirizine Dihydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
17511-106
2020-01-20
2024-12-31
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Levocetirizine Dihydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
66039-837
2009-03-31
2024-12-31
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(R)-Cetirizine Dihydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
24234-0004
2017-05-15
2024-12-31
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Levocetirizine dihydrochloride
POWDER (25kg/25kg)
BULK INGREDIENT
62207-009
2018-09-13
2024-12-31
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LEVOCETIRIZINE DIHYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT
49574-521
2019-06-01
2024-12-31
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Levocetirizine dihydrochloride
POWDER (1kg/kg)
BULK INGREDIENT FOR ...
49574-632
2005-03-02
2024-12-31
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levocetirizine dihydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
65372-1161
2011-09-26
2024-12-31
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Levocetirizine Dihydrochloride
POWDER (1g/g)
BULK INGREDIENT FOR ...
62991-3149
2019-08-08
2024-12-31
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LEVOCETIRIZINE DIHYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT FOR ...
51927-5050
2019-03-25
2024-12-31
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Levocetirizine Dihydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
66022-0108
2008-01-28
2024-12-31
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Levocetirizine Dihydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
66022-0108
2008-01-28
2024-12-31
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levocetirizine dihydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
28877-5801
2009-11-12
2024-12-31
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  • SOLUTION;ORAL - 2.5MG/5ML
  • TABLET;ORAL - 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • SOLUTION;ORAL - 2.5MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Looking for 130018-87-0 / Levocetirizine Dihydrochloride API manufacturers, exporters & distributors?

Levocetirizine Dihydrochloride manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Levocetirizine Dihydrochloride 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 Levocetirizine Dihydrochloride manufacturer or Levocetirizine Dihydrochloride supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levocetirizine Dihydrochloride manufacturer or Levocetirizine Dihydrochloride supplier.

PharmaCompass also assists you with knowing the Levocetirizine Dihydrochloride API Price utilized in the formulation of products. Levocetirizine Dihydrochloride API Price is not always fixed or binding as the Levocetirizine Dihydrochloride Price is obtained through a variety of data sources. The Levocetirizine Dihydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Levocetirizine Dihydrochloride

Synonyms

130018-87-0, Xyzal, Xusal, (r)-cetirizine dihydrochloride, Levocetirizine hcl, Levocetirizine dihydrochloride [usan]

Cas Number

130018-87-0

Unique Ingredient Identifier (UNII)

SOD6A38AGA

About Levocetirizine Dihydrochloride

Levocetirizine Dihydrochloride is the dihydrochloride salt form of the active levorotatory enantiomer of cetirizine, levocetirizine; a third generation, non-sedating, selective histamine H1 receptor antagonist, with antihistamine, anti-inflammatory and potential anti-angiogenic activities. Levocetirizine competes with endogenous histamine for binding at peripheral H1-receptor sites on the effector cell surface. This prevents the negative symptoms associated with histamine release and an allergic reaction. In addition, as histamine plays an important role in angiogenesis during an allergic inflammatory reaction, blocking the action of histamine may modulate the expression of proangiogenic factors and thus may prevent angiogenesis. As a third-generation histamine H1 receptor antagonist, levocetirizine has fewer side effects than most second-generation antihistamines.

Levocetirizine Manufacturers

A Levocetirizine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levocetirizine, including repackagers and relabelers. The FDA regulates Levocetirizine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levocetirizine 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 Levocetirizine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Levocetirizine Suppliers

A Levocetirizine supplier is an individual or a company that provides Levocetirizine active pharmaceutical ingredient (API) or Levocetirizine finished formulations upon request. The Levocetirizine suppliers may include Levocetirizine API manufacturers, exporters, distributors and traders.

click here to find a list of Levocetirizine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Levocetirizine NDC

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 Levocetirizine as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Levocetirizine API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 Levocetirizine 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Levocetirizine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Levocetirizine NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Levocetirizine suppliers with NDC on PharmaCompass.

Levocetirizine Manufacturers | Traders | Suppliers

Levocetirizine Manufacturers, Traders, Suppliers 1
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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