Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.

Reset all filters
01 1Supriya Lifescience Limited
02 1Wavelength Enterprises LTD
03 1Granules India Limited
04 1COSMA Spa
05 1Willow Birch Pharma, LLC
06 1AX Pharmaceutical Corp
07 1Arch Pharmalabs Limited
08 1Bajaj Healthcare Ltd
09 1Calyx Chemicals & Pharmaceuticals Limited
10 2Cipla Ltd.
11 1Glochem Industries Private Limited
12 1Ipca Laboratories Limited
13 1Jubilant Biosys limited
14 1Kalchem International inc
15 2Matrix Pharmacorp Private Limited
16 1PRAVEEN LABORATORIES PRIVATE LIMITED
17 1PROFESSIONAL COMPOUNDING CENTERS OF AMERICA
18 1SUN PHARMACEUTICAL INDUSTRIES, INC.
19 1THINQ Pharma-CRO Limited
20 1UCB Farchim S.A.
21 1Unichem Laboratories Limited, India
Reset all filters
01 1CETIRIZINE DIHYDROCHLORIDE
02 1CETIRIZINE HCL
03 3CETIRIZINE HYDROCHLORIDE
04 5Cetirizine Dihydrochloride
05 10Cetirizine Hydrochloride
06 1Cetirizine hydrochloride
07 2cetirizine hydrochloride
Reset all filters
01 1Canada
02 13India
03 1Israel
04 1Italy
05 1Switzerland
06 4U.S.A
07 1United Kingdom
08 1Blank
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 : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58175-0370
Start Marketing Date : 2001-02-09
End Marketing Date : 2027-12-31
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 : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
Cosma S.p.A., part of CFM Group with AMSA & Clarochem, provides global pharma & veterinary health with 300+ tons of FDA-approved APIs.
CETIRIZINE DIHYDROCHLORIDE, (S)-
NDC Package Code : 51604-0021
Start Marketing Date : 2018-11-26
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Willow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.
NDC Package Code : 10695-143
Start Marketing Date : 2022-11-16
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22365-111
Start Marketing Date : 2010-01-11
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT

NDC Package Code : 53104-7528
Start Marketing Date : 2016-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT

CETIRIZINE DIHYDROCHLORIDE, (S)-
NDC Package Code : 24234-0001
Start Marketing Date : 2006-06-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

NDC Package Code : 51927-5282
Start Marketing Date : 2025-06-11
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...

NDC Package Code : 28877-1227
Start Marketing Date : 2010-06-21
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

63
PharmaCompass offers a list of Cetirizine Dihydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Cetirizine Dihydrochloride manufacturer or Cetirizine Dihydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cetirizine Dihydrochloride manufacturer or Cetirizine Dihydrochloride supplier.
A Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard, including repackagers and relabelers. The FDA regulates Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard 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, United States Pharmacopeia (USP) Reference Standard manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard supplier is an individual or a company that provides Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard active pharmaceutical ingredient (API) or Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard finished formulations upon request. The Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard suppliers may include Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard API manufacturers, exporters, distributors and traders.
click here to find a list of Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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, United States Pharmacopeia (USP) Reference Standard as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard 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, United States Pharmacopeia (USP) Reference Standard 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, United States Pharmacopeia (USP) Reference Standard and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard suppliers with NDC on PharmaCompass.
We have 20 companies offering Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard
Get in contact with the supplier of your choice: