Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1Farmak, a,s
02 1Dr. Reddy's Laboratories Limited
03 1MYLAN LABORATORIES LIMITED
04 1Medisca Inc.
05 1Professional Compounding Centers of America dba PCCA
06 1Symed Labs Limited
07 1Unichem Laboratories Limited, India
01 2TIZANIDINE HYDROCHLORIDE
02 5Tizanidine Hydrochloride
01 1Czech Republic
02 3India
03 2U.S.A
04 1United Kingdom
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
NDC Package Code : 63278-0489
Start Marketing Date : 2003-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-020
Start Marketing Date : 2001-11-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-2351
Start Marketing Date : 2014-03-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0020
Start Marketing Date : 2014-04-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 66022-0202
Start Marketing Date : 1996-11-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-003
Start Marketing Date : 2001-11-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-777
Start Marketing Date : 2015-02-19
End Marketing Date : 2026-12-01
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Tizanidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tizanidine Hydrochloride, including repackagers and relabelers. The FDA regulates Tizanidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tizanidine 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 Tizanidine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tizanidine Hydrochloride supplier is an individual or a company that provides Tizanidine Hydrochloride active pharmaceutical ingredient (API) or Tizanidine Hydrochloride finished formulations upon request. The Tizanidine Hydrochloride suppliers may include Tizanidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Tizanidine 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 Tizanidine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tizanidine 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 Tizanidine 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 Tizanidine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tizanidine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tizanidine Hydrochloride suppliers with NDC on PharmaCompass.
We have 7 companies offering Tizanidine Hydrochloride
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