Suanfarma, at the Core of a Better Life.
01 1CIPAN-Companhia Industrial Produtora de Antibióticos, S.A.
02 1AX Pharmaceutical Corp
03 2Curia Italy S.r.l.
04 1DARMERICA, LLC
05 1Fagron Services BV
06 2Hovione FarmaCiencia SA
07 1KALCHEM INTERNATIONAL INC.
08 1Professional Compounding Centers of America dba PCCA
09 1Zhejiang Changhai Pharmaceuticals Co., Ltd.
10 1Zhejiang Hisun Pharmaceutical Co., Ltd.
01 1MINOCYCLINE
02 2MINOCYCLINE HYDROCHLORIDE
03 1Minocycline HCL
04 1Minocycline HCl
05 1Minocycline Hcl Dihydrate
06 6Minocycline Hydrochloride
01 1Canada
02 2China
03 1Netherlands
04 2Portugal
05 1Spain
06 4U.S.A
07 1United Kingdom
Suanfarma, at the Core of a Better Life.
NDC Package Code : 17158-0900
Start Marketing Date : 2017-03-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 73377-221
Start Marketing Date : 2023-02-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 44657-0051
Start Marketing Date : 2010-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (30kg/30kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 44657-0081
Start Marketing Date : 2019-10-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (30kg/30kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-122
Start Marketing Date : 2021-11-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50909-9101
Start Marketing Date : 1993-07-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50909-9201
Start Marketing Date : 2015-01-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60592-918
Start Marketing Date : 2023-10-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-2197
Start Marketing Date : 2013-06-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 58623-0133
Start Marketing Date : 2019-09-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Minocycline, Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Minocycline, Hydrochloride, including repackagers and relabelers. The FDA regulates Minocycline, Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Minocycline, 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 Minocycline, Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Minocycline, Hydrochloride supplier is an individual or a company that provides Minocycline, Hydrochloride active pharmaceutical ingredient (API) or Minocycline, Hydrochloride finished formulations upon request. The Minocycline, Hydrochloride suppliers may include Minocycline, Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Minocycline, 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 Minocycline, Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Minocycline, 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 Minocycline, 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 Minocycline, Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Minocycline, Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Minocycline, Hydrochloride suppliers with NDC on PharmaCompass.
We have 10 companies offering Minocycline, Hydrochloride
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