Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1Wavelength Enterprises LTD
02 1Dr.Reddy's Laboratories Limited
03 1Supriya Lifescience Limited
04 1Granules India Limited
05 1AX Pharmaceutical Corp
06 1Arch Pharmalabs Limited
07 1COSMA Spa
08 1Calyx Chemicals & Pharmaceuticals Limited
09 2Cipla Ltd.
10 1Glochem Industries Private Limited
11 1Ipca Laboratories Limited
12 1Jubilant Pharmova Limited
13 1Kalchem International inc
14 1MYLAN LABORATORIES LIMITED
15 1Mylan Laboratories Limited
16 1THINQ Pharma-CRO Limited
17 2Tianish Laboratories Private Limited
18 1UCB Farchim S.A.
19 1Unichem Laboratories Limited, India
01 1CETIRIZINE DIHYDROCHLORIDE
02 1CETIRIZINE HCL
03 4CETIRIZINE HYDROCHLORIDE
04 1Cetirizine
05 4Cetirizine Dihydrochloride
06 7Cetirizine Hydrochloride
07 1Cetirizine hydrochloride
08 2cetirizine hydrochloride
01 1Canada
02 1France
03 14India
04 1Italy
05 1Switzerland
06 3U.S.A
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
NDC Package Code : 58175-0370
Start Marketing Date : 2001-02-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 71796-013
Start Marketing Date : 2005-05-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
NDC Package Code : 61281-4250
Start Marketing Date : 2017-08-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
NDC Package Code : 62207-001
Start Marketing Date : 2016-12-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/1)
Marketing Category : EXPORT ONLY
NDC Package Code : 22365-111
Start Marketing Date : 2010-01-11
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7528
Start Marketing Date : 2016-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7528
Start Marketing Date : 2018-12-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT
CETIRIZINE DIHYDROCHLORIDE, (S)-
NDC Package Code : 51604-0021
Start Marketing Date : 2018-11-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
CETIRIZINE DIHYDROCHLORIDE, (S)-
NDC Package Code : 24234-0001
Start Marketing Date : 2006-06-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 28877-1227
Start Marketing Date : 2010-06-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Cetirizine Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cetirizine Dihydrochloride, including repackagers and relabelers. The FDA regulates Cetirizine Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cetirizine 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 Cetirizine Dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cetirizine Dihydrochloride supplier is an individual or a company that provides Cetirizine Dihydrochloride active pharmaceutical ingredient (API) or Cetirizine Dihydrochloride finished formulations upon request. The Cetirizine Dihydrochloride suppliers may include Cetirizine Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Cetirizine 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 Cetirizine Dihydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cetirizine 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 Cetirizine 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 Cetirizine Dihydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cetirizine Dihydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cetirizine Dihydrochloride suppliers with NDC on PharmaCompass.
We have 18 companies offering Cetirizine Dihydrochloride
Get in contact with the supplier of your choice:
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