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USA Home > Product Directory > Analytical/Chromatography > Analytical Standards > Chromatography > Pharmaceutical Standards > Pharmaceutical Impurities

Fluka and Supelco
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Pharmaceutical Impurities

Pharmaceutical impurities may have a significant influence on the effects of a drug or may cause unwanted side-effects. Guidelines and limits for many impurities are described in the pharmacopeia monographs.
The Fluka branded Pharmaceutical Impurity Standards specifications generally include Chromatographic purity, water content, residual solvents and structure confirmation by NMR.
  • Aspirin (Acetylsalicyclic Acid) Impurities - (1)
  • Betamethasone valerate Impurities - (2)
  • Bupropion Impurities - (2)
  • Carvedilol Impurities - (6)
  • Ciprofloxacin Hydrochloride Impurities - (1)
  • Clobetasol-17-propionate Impurities - (3)
  • Clotrimazole Impurities - (2)
  • Guaifenesin Impurities - (1)
  • Hydrochlorothiazide Impurities - (2)
  • Ibuprofen Impurities - (1)
  • Lamotrigine Impurities - (3)
  • Metformin hydrochloride Impurities - (2)
  • Metronidazole Impurities - (1)
  • N-Acetyl-L-Tyrosine Impurities - (1)
  • Ondansetron hydrochloride Impurities - (8)
  • Paracetamol (Acetaminophen) Impurities - (3)
  • Ranitidine hydrochloride Impurities - (2)
  • Salicylic Acid Impurities - (1)
  • Sulfamethoxazole - (1)
  • Valaciclovir impurities - (5)
  • Verapamil Hydrochloride Impurities - (2)

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