01 1C-squared Pharma Sarl
01 1pilocarpine nitrate
01 1Ireland
NDC Package Code : 69205-002
Start Marketing Date : 2014-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Pilocarpine Nitrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pilocarpine Nitrate, including repackagers and relabelers. The FDA regulates Pilocarpine Nitrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pilocarpine Nitrate 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 Pilocarpine Nitrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pilocarpine Nitrate supplier is an individual or a company that provides Pilocarpine Nitrate active pharmaceutical ingredient (API) or Pilocarpine Nitrate finished formulations upon request. The Pilocarpine Nitrate suppliers may include Pilocarpine Nitrate API manufacturers, exporters, distributors and traders.
click here to find a list of Pilocarpine Nitrate 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 Pilocarpine Nitrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pilocarpine Nitrate 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 Pilocarpine Nitrate 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 Pilocarpine Nitrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pilocarpine Nitrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Pilocarpine Nitrate suppliers with NDC on PharmaCompass.
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