01 1Chifeng Pharmaceutical Co.,Ltd
02 1DARMERICA, LLC
03 1Kalchem International inc
04 1Spectrum Laboratory Products, Inc.
01 1GRISEOFULVIN
02 3Griseofulvin
01 1China
02 3U.S.A
NDC Package Code : 71052-109
Start Marketing Date : 2022-10-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60592-306
Start Marketing Date : 2019-11-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 60264-310
Start Marketing Date : 2007-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-3363
Start Marketing Date : 2000-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A GRISEOFULVIN, ULTRAMICROSIZE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of GRISEOFULVIN, ULTRAMICROSIZE, including repackagers and relabelers. The FDA regulates GRISEOFULVIN, ULTRAMICROSIZE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. GRISEOFULVIN, ULTRAMICROSIZE 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 GRISEOFULVIN, ULTRAMICROSIZE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A GRISEOFULVIN, ULTRAMICROSIZE supplier is an individual or a company that provides GRISEOFULVIN, ULTRAMICROSIZE active pharmaceutical ingredient (API) or GRISEOFULVIN, ULTRAMICROSIZE finished formulations upon request. The GRISEOFULVIN, ULTRAMICROSIZE suppliers may include GRISEOFULVIN, ULTRAMICROSIZE API manufacturers, exporters, distributors and traders.
click here to find a list of GRISEOFULVIN, ULTRAMICROSIZE 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 GRISEOFULVIN, ULTRAMICROSIZE as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for GRISEOFULVIN, ULTRAMICROSIZE 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 GRISEOFULVIN, ULTRAMICROSIZE 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 GRISEOFULVIN, ULTRAMICROSIZE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a GRISEOFULVIN, ULTRAMICROSIZE NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of GRISEOFULVIN, ULTRAMICROSIZE suppliers with NDC on PharmaCompass.
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