01 1Apotheca Company
01 1Sarcolacticum acidum
01 1U.S.A
NDC Package Code : 57520-1262
Start Marketing Date : 2014-02-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (3g)
Marketing Category : DRUG FOR FURTHER PROCESSING
A Lactic acid, L- manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lactic acid, L-, including repackagers and relabelers. The FDA regulates Lactic acid, L- manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lactic acid, L- 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 Lactic acid, L- supplier is an individual or a company that provides Lactic acid, L- active pharmaceutical ingredient (API) or Lactic acid, L- finished formulations upon request. The Lactic acid, L- suppliers may include Lactic acid, L- API manufacturers, exporters, distributors and traders.
click here to find a list of Lactic acid, L- 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 Lactic acid, L- as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lactic acid, L- 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 Lactic acid, L- 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 Lactic acid, L- and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lactic acid, L- NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lactic acid, L- suppliers with NDC on PharmaCompass.
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