Coral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics.
01 1Coral Drugs Private Limited
02 1Evonik Operations GmbH
03 1AX Pharmaceutical Corp
04 1Curia Italy S.r.l.
05 1DARMERICA, LLC
06 1Daito Pharmaceutical Co., Ltd
07 1Esteve Quimica, SA
08 1LETCO MEDICAL, LLC
09 1MSN Laboratories Private Limited
10 1Professional Compounding Centers of America
11 1Professional Compounding Centers of America dba PCCA
12 1Urquima, S.A.
13 1Zhejiang Lepu Pharmaceutical Co., Ltd.
14 1Zydus Lifesciences Limited
01 3AZELASTINE HYDROCHLORIDE
02 2Azelastine HCl
03 9Azelastine Hydrochloride
01 1Canada
02 1China
03 1Germany
04 3India
05 1Japan
06 2Spain
07 3U.S.A
08 2United Kingdom
Coral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics.
NDC Package Code : 49076-7601
Start Marketing Date : 2019-06-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
NDC Package Code : 49274-1101
Start Marketing Date : 2001-05-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55486-1575
Start Marketing Date : 2012-06-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60656-1839
Start Marketing Date : 2006-06-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57572-0713
Start Marketing Date : 2007-09-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-3200
Start Marketing Date : 2023-11-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 14501-0048
Start Marketing Date : 2010-03-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0302
Start Marketing Date : 2023-04-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-5005
Start Marketing Date : 2018-01-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 54752-0008
Start Marketing Date : 2000-05-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Viatris brand of azelastine hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Viatris brand of azelastine hydrochloride, including repackagers and relabelers. The FDA regulates Viatris brand of azelastine hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Viatris brand of azelastine hydrochloride 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 Viatris brand of azelastine hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Viatris brand of azelastine hydrochloride supplier is an individual or a company that provides Viatris brand of azelastine hydrochloride active pharmaceutical ingredient (API) or Viatris brand of azelastine hydrochloride finished formulations upon request. The Viatris brand of azelastine hydrochloride suppliers may include Viatris brand of azelastine hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Viatris brand of azelastine hydrochloride 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 Viatris brand of azelastine hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Viatris brand of azelastine hydrochloride 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 Viatris brand of azelastine hydrochloride 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 Viatris brand of azelastine hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Viatris brand of azelastine hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Viatris brand of azelastine hydrochloride suppliers with NDC on PharmaCompass.
We have 13 companies offering Viatris brand of azelastine hydrochloride
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