Xellia Delivering Reliable Anti-Infective Solutions Through Expertise, Quality, and Uninterrupted Global Supply.
01 2Xellia (Taizhou) Pharmaceuticals Co., Ltd
02 2Xellia (Taizhou) Pharmaceuticals Co., Ltd.
03 1Xellia Pharmaceuticals ApS
04 2Josun International Limited
05 2Joyang Laboratories
06 4Lifecome Biochemistry Co., Ltd
07 1Medisca Inc.
08 2North China Pharmaceutical Huasheng Co. Ltd.
09 1Professional Compounding Centers of America dba PCCA
01 1BACITRACIN ZINC
02 6Bacitracin
03 7Bacitracin Zinc
04 2bacitracin
05 1bacitracin zinc
01 6China
02 5Denmark
03 1U.S.A
04 1United Kingdom
05 4Blank
Xellia Delivering Reliable Anti-Infective Solutions Through Expertise, Quality, and Uninterrupted Global Supply.
NDC Package Code : 44231-0002
Start Marketing Date : 2012-12-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Xellia Delivering Reliable Anti-Infective Solutions Through Expertise, Quality, and Uninterrupted Global Supply.
NDC Package Code : 44231-0005
Start Marketing Date : 2012-12-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Xellia Delivering Reliable Anti-Infective Solutions Through Expertise, Quality, and Uninterrupted Global Supply.
NDC Package Code : 44231-0003
Start Marketing Date : 2012-12-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Xellia Delivering Reliable Anti-Infective Solutions Through Expertise, Quality, and Uninterrupted Global Supply.
NDC Package Code : 45932-0022
Start Marketing Date : 2015-07-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Xellia Delivering Reliable Anti-Infective Solutions Through Expertise, Quality, and Uninterrupted Global Supply.
NDC Package Code : 44231-0004
Start Marketing Date : 2012-12-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0015
Start Marketing Date : 2013-03-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 41699-1000
Start Marketing Date : 2026-02-09
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 41699-2000
Start Marketing Date : 2024-12-16
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 41699-1000
Start Marketing Date : 2024-12-16
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 41699-2000
Start Marketing Date : 2026-02-09
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
21
PharmaCompass offers a list of Bacitracin Zinc 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 Bacitracin Zinc manufacturer or Bacitracin Zinc supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bacitracin Zinc manufacturer or Bacitracin Zinc supplier.
A ZIBA-RX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ZIBA-RX, including repackagers and relabelers. The FDA regulates ZIBA-RX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ZIBA-RX 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 ZIBA-RX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A ZIBA-RX supplier is an individual or a company that provides ZIBA-RX active pharmaceutical ingredient (API) or ZIBA-RX finished formulations upon request. The ZIBA-RX suppliers may include ZIBA-RX API manufacturers, exporters, distributors and traders.
click here to find a list of ZIBA-RX 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 ZIBA-RX as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for ZIBA-RX 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 ZIBA-RX 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 ZIBA-RX and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a ZIBA-RX NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of ZIBA-RX suppliers with NDC on PharmaCompass.
We have 6 companies offering ZIBA-RX
Get in contact with the supplier of your choice:
