Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
01 1Chunghwa Chemical Synthesis & Biotech. Ltd
02 1AX Pharmaceutical Corp
03 2Biocon Limited
04 1CKD Bio Corporation
05 4Concord Biotech Limited
06 1Curia Italy S.r.l.
07 1Darmerica LLC
08 2Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd
09 1Hisun Pharmaceutical (Hangzhou) Co., Ltd.
10 1Joyang Laboratories
11 1LETCO MEDICAL, LLC
12 1Medisca Inc.
13 1North China Pharmaceutical Huasheng Co. Ltd.
14 1Novartis Pharmaceuticals Corporation
15 1Professional Compounding Centers of America
16 1Professional Compounding Centers of America dba PCCA
17 1TAPI Czech Industries s.r.o.
18 1Teva Czech Industries s.r.o
19 1Wuxi Fortune Pharmaceutical Co.,Ltd.
01 2TACROLIMUS
02 1TACROLIMUS MONOHYDRATE
03 18Tacrolimus
04 1Tacrolimus Monohydrate
05 1Tacrolimus Premix 20 %
06 1tacrolimus
01 1Canada
02 6China
03 6India
04 1Israel
05 1South Korea
06 1Switzerland
07 1Taiwan
08 4U.S.A
09 2United Kingdom
10 1Blank
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
NDC Package Code : 52076-6222
Start Marketing Date : 2017-05-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52972-0040
Start Marketing Date : 2016-09-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55486-1576
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 : 51187-0006
Start Marketing Date : 2019-09-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52928-006
Start Marketing Date : 2021-11-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-2698
Start Marketing Date : 2012-11-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0078-1399
Start Marketing Date : 2009-08-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0092
Start Marketing Date : 2020-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0209
Start Marketing Date : 2021-08-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 47848-018
Start Marketing Date : 2020-05-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
A Tacrolimus Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tacrolimus Monohydrate, including repackagers and relabelers. The FDA regulates Tacrolimus Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tacrolimus Monohydrate 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 Tacrolimus Monohydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tacrolimus Monohydrate supplier is an individual or a company that provides Tacrolimus Monohydrate active pharmaceutical ingredient (API) or Tacrolimus Monohydrate finished formulations upon request. The Tacrolimus Monohydrate suppliers may include Tacrolimus Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Tacrolimus Monohydrate 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 Tacrolimus Monohydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tacrolimus Monohydrate 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 Tacrolimus Monohydrate 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 Tacrolimus Monohydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tacrolimus Monohydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tacrolimus Monohydrate suppliers with NDC on PharmaCompass.
We have 17 companies offering Tacrolimus Monohydrate
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