01 1AX Pharmaceutical Corp
02 1Alembic Pharmaceuticals Limited
03 1Anuh Pharma Ltd.
04 2Calyx Chemicals & Pharmaceuticals
05 1DARMERICA, LLC
06 1HEC PHARM CO., LTD
07 1Jiangsu Weiqida Pharmaceutical Co., Ltd.
08 2Jubilant Pharmova Limited
09 1Kopran Research Laboratories Limited
10 1LETCO MEDICAL, LLC
11 1Medisca Inc.
12 1Ningxia Qiyuan Pharmaceutical Co., Ltd.
13 1Pfizer Asia Manufacturing Pte Ltd
14 2Professional Compounding Centers of America
15 1TAPI Croatia Industries Ltd.
16 1Viatris Pharmaceuticals LLC
17 1ZHEJIANG GUOBANG PHARMACEUTICAL CO., LTD.
01 1AZITHROMYCIN
02 3AZITHROMYCIN DIHYDRATE
03 1AZITHROMYCIN MONOHYDRATE
04 3Azithromycin
05 6Azithromycin Dihydrate
06 2Azithromycin Monohydrate
07 2Azithromycin dihydrate
08 1Azithromycine Dihydrate
09 1azithromycin dihydrate
01 1Canada
02 3China
03 6India
04 5U.S.A
05 2United Kingdom
06 3Blank
NDC Package Code : 46708-866
Start Marketing Date : 2011-01-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 43781-0305
Start Marketing Date : 2015-10-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61294-9990
Start Marketing Date : 2020-04-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-2246
Start Marketing Date : 2014-07-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59566-0124
Start Marketing Date : 2016-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0182
Start Marketing Date : 2019-04-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0307
Start Marketing Date : 2023-08-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51943-120
Start Marketing Date : 2023-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 11722-042
Start Marketing Date : 2017-12-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 58326-2171
Start Marketing Date : 2021-06-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Azithromycin Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azithromycin Dihydrate, including repackagers and relabelers. The FDA regulates Azithromycin Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azithromycin Dihydrate 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 Azithromycin Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Azithromycin Dihydrate supplier is an individual or a company that provides Azithromycin Dihydrate active pharmaceutical ingredient (API) or Azithromycin Dihydrate finished formulations upon request. The Azithromycin Dihydrate suppliers may include Azithromycin Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Azithromycin Dihydrate 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 Azithromycin Dihydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Azithromycin Dihydrate 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 Azithromycin Dihydrate 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 Azithromycin Dihydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Azithromycin Dihydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Azithromycin Dihydrate suppliers with NDC on PharmaCompass.
We have 14 companies offering Azithromycin Dihydrate
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