01 1Schwabe Mexico S.A. de C.V.
02 1Schwabe North America
01 2ACONITUM NAPELLUS, BRYONIA ALBA ROOT, CALCIUM SULFIDE, SPONGIA OFFICINALIS SKELETON, ROASTED, STANNOUS CATION
01 1Mexico
02 1U.S.A
ACONITUM NAPELLUS; BRYONIA ALBA ROOT; CALCIUM SULFIDE; SPONGIA OFFICINALIS SKELETON, ROASTED; STANNOUS CATION
NDC Package Code : 53499-2090
Start Marketing Date : 2020-12-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (320kg 320kg 620kg 320kg 620kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
ACONITUM NAPELLUS; BRYONIA ALBA ROOT; CALCIUM SULFIDE; SPONGIA OFFICINALIS SKELETON, ROASTED; STANNOUS CATION
NDC Package Code : 68466-1974
Start Marketing Date : 2020-12-18
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (320kg 320kg 620kg 320kg 620kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
A Calcium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Calcium, including repackagers and relabelers. The FDA regulates Calcium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Calcium API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Calcium supplier is an individual or a company that provides Calcium active pharmaceutical ingredient (API) or Calcium finished formulations upon request. The Calcium suppliers may include Calcium API manufacturers, exporters, distributors and traders.
click here to find a list of Calcium 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 Calcium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Calcium 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 Calcium 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 Calcium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Calcium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Calcium suppliers with NDC on PharmaCompass.
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