01 1Formosa Laboratories, Inc.
01 1Ergocalciferol
01 1Taiwan
NDC Package Code : 66499-0041
Start Marketing Date : 2010-02-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Ergocalciferol, British Pharmacopoeia (BP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ergocalciferol, British Pharmacopoeia (BP) Reference Standard, including repackagers and relabelers. The FDA regulates Ergocalciferol, British Pharmacopoeia (BP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ergocalciferol, British Pharmacopoeia (BP) Reference Standard API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Ergocalciferol, British Pharmacopoeia (BP) Reference Standard supplier is an individual or a company that provides Ergocalciferol, British Pharmacopoeia (BP) Reference Standard active pharmaceutical ingredient (API) or Ergocalciferol, British Pharmacopoeia (BP) Reference Standard finished formulations upon request. The Ergocalciferol, British Pharmacopoeia (BP) Reference Standard suppliers may include Ergocalciferol, British Pharmacopoeia (BP) Reference Standard API manufacturers, exporters, distributors and traders.
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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 Ergocalciferol, British Pharmacopoeia (BP) Reference Standard as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ergocalciferol, British Pharmacopoeia (BP) Reference Standard 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 Ergocalciferol, British Pharmacopoeia (BP) Reference Standard 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 Ergocalciferol, British Pharmacopoeia (BP) Reference Standard and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ergocalciferol, British Pharmacopoeia (BP) Reference Standard NDC to their finished compounded human drug products, they may choose to do so.
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