01 1CSPC Weisheng Pharmaceutical (Shijiazhuang) Co., Ltd
02 2DSM Nutritional Products Ltd.
03 1Medisca Inc.
04 1Spectrum Laboratory Products, Inc.
01 2ASCORBIC ACID
02 2Ascorbic Acid
03 1Ascorbic acid
01 1China
02 2Netherlands
03 2U.S.A
NDC Package Code : 72783-1001
Start Marketing Date : 2020-04-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-3301
Start Marketing Date : 2024-05-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 63238-3000
Start Marketing Date : 2017-12-20
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63238-3000
Start Marketing Date : 2022-12-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-0742
Start Marketing Date : 2021-06-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Ascorbic Acid API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Ascorbic Acid manufacturer or Ascorbic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ascorbic Acid manufacturer or Ascorbic Acid supplier.
PharmaCompass also assists you with knowing the Ascorbic Acid API Price utilized in the formulation of products. Ascorbic Acid API Price is not always fixed or binding as the Ascorbic Acid Price is obtained through a variety of data sources. The Ascorbic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A M.V.I. ADULT (PHARMACY BULK PACKAGE) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of M.V.I. ADULT (PHARMACY BULK PACKAGE), including repackagers and relabelers. The FDA regulates M.V.I. ADULT (PHARMACY BULK PACKAGE) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. M.V.I. ADULT (PHARMACY BULK PACKAGE) 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 M.V.I. ADULT (PHARMACY BULK PACKAGE) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A M.V.I. ADULT (PHARMACY BULK PACKAGE) supplier is an individual or a company that provides M.V.I. ADULT (PHARMACY BULK PACKAGE) active pharmaceutical ingredient (API) or M.V.I. ADULT (PHARMACY BULK PACKAGE) finished formulations upon request. The M.V.I. ADULT (PHARMACY BULK PACKAGE) suppliers may include M.V.I. ADULT (PHARMACY BULK PACKAGE) API manufacturers, exporters, distributors and traders.
click here to find a list of M.V.I. ADULT (PHARMACY BULK PACKAGE) 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 M.V.I. ADULT (PHARMACY BULK PACKAGE) as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for M.V.I. ADULT (PHARMACY BULK PACKAGE) 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 M.V.I. ADULT (PHARMACY BULK PACKAGE) 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 M.V.I. ADULT (PHARMACY BULK PACKAGE) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a M.V.I. ADULT (PHARMACY BULK PACKAGE) NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of M.V.I. ADULT (PHARMACY BULK PACKAGE) suppliers with NDC on PharmaCompass.
We have 4 companies offering M.V.I. ADULT (PHARMACY BULK PACKAGE)
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