01 1Cambridge Isotope Laboratories
01 1U.S.A
01 1Blank
01 1Blank
01 1221MF10045
01 1Blank
Registration Number : 221MF10045
Registrant's Address : 3 Highwood Drive, Tewksbury, MA 01876, USA
Initial Date of Registration : 2009-02-25
Latest Date of Registration : --
NDC Package Code : 61444-901
Start Marketing Date : 1996-02-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER, FOR SOLUTION (1g/g)
Marketing Category : BULK INGREDIENT
A UREA C-13 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UREA C-13, including repackagers and relabelers. The FDA regulates UREA C-13 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UREA C-13 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 UREA C-13 supplier is an individual or a company that provides UREA C-13 active pharmaceutical ingredient (API) or UREA C-13 finished formulations upon request. The UREA C-13 suppliers may include UREA C-13 API manufacturers, exporters, distributors and traders.
click here to find a list of UREA C-13 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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