HealthTech BioActives, leading globally in Flavonoids and Vitamin B12 Derivatives.
01 1HEALTHTECH BIOACTIVES SL
02 2Supriya Lifescience Limited
03 1AX Pharmaceutical Corp
04 1BHAGERIA & JAJODIA PHARMACEUTICALS PRIVATE LIMITED
05 1Darmerica, LLC
06 1Fagron Inc
07 1Professional Compounding Centers of America
08 1Spectrum Laboratory Products, Inc.
09 2Willow Birch Pharma, Inc.
01 3METHYLCOBALAMIN
02 1Mecobalamin
03 7Methylcobalamin
01 1Canada
02 2India
03 1Netherlands
04 1Spain
05 4U.S.A
06 1United Kingdom
07 1Blank
HealthTech BioActives, leading globally in Flavonoids and Vitamin B12 Derivatives.
NDC Package Code : 84069-001
Start Marketing Date : 2024-02-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
NDC Package Code : 61281-9000
Start Marketing Date : 2013-09-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
NDC Package Code : 61281-9500
Start Marketing Date : 2013-09-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 73377-286
Start Marketing Date : 2024-09-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 71052-047
Start Marketing Date : 2017-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-1609
Start Marketing Date : 2021-06-17
End Marketing Date : 2026-02-28
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0220
Start Marketing Date : 2021-12-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-4659
Start Marketing Date : 2015-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10695-174
Start Marketing Date : 2023-01-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10695-174
Start Marketing Date : 2023-06-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Methylcobalamin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methylcobalamin, including repackagers and relabelers. The FDA regulates Methylcobalamin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methylcobalamin 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 Methylcobalamin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methylcobalamin supplier is an individual or a company that provides Methylcobalamin active pharmaceutical ingredient (API) or Methylcobalamin finished formulations upon request. The Methylcobalamin suppliers may include Methylcobalamin API manufacturers, exporters, distributors and traders.
click here to find a list of Methylcobalamin 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 Methylcobalamin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Methylcobalamin 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 Methylcobalamin 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 Methylcobalamin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Methylcobalamin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Methylcobalamin suppliers with NDC on PharmaCompass.
We have 8 companies offering Methylcobalamin
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