JOST CHEMICAL CO

St. Louis, Missouri, United States jostchemical.com

Overview

JOST CHEMICAL CO is an active pharmaceutical ingredient (API) supplier with 16 active FDA Type II Drug Master Files, covering MAGNESIUM CITRATE TRIBASIC ANHYDROUS; MAGNESIUM LACTATE DIHYDRATE; MAGNESIUM SULFATE ANHYDROUS; MAGNESIUM SULFATE DRIED; MANGANESE SULFATE MONOHYDRATE; POTASSIUM PHOSPHATE DIBASIC (3673).

Core services & business areas

API ManufacturingPharmaceutical Manufacturing

Active pharmaceutical ingredients supplied

Substances JOST CHEMICAL CO is evidenced to supply (US FDA Drug Master File or EU CEP). Open any ingredient to see its full supplier landscape, CAS number and patent status.

PotassiumCalciumMagnesiumPotassium Phosphate, DibasicZinc OxidePotassium SulfatePotassium Phosphate, MonobasicManganese SulfatePotassium NitrateMagnesium Sulfate AnhydrousSodium Sulfate AnhydrousMagnesium Citrate

API / Drug Master Files

JOST CHEMICAL CO holds 15 active (25 total) FDA Type II Drug Master Files — identifying it as an active-substance / API supplier. Type II DMFs are filed with the FDA to support the use of an active pharmaceutical ingredient in drug applications.

  • SODIUM PHOSPHATE MONOBASIC MONOHYDRATEActive2022-06-30
  • SODIUM PHOSPHATE DIBASIC HEPTAHYDRATEActive2022-06-29
  • POTASSIUM PHOSPHATE DIBASIC (3673)Active2020-09-29
  • POTASSIUM PHOSPHATE MONOBASIC (3674)Active2020-09-22
  • ZINC SULFATE HEPTAHYDRATEActive2020-08-11
  • MAGNESIUM SULFATE ANHYDROUSActive2020-04-17
  • SODIUM SULFATE ANHYDROUS (3808)Active2019-02-21
  • MANGANESE SULFATE MONOHYDRATEActive2016-04-07
  • SODIUM PHOSPHATE DIBASIC DIHYDRATEActive2013-08-14
  • SODIUM PHOSPHATE MONOBASIC, MONOHYDRATEActive2011-07-05
  • MAGNESIUM SULFATE DRIEDActive2011-07-05
  • SODIUM PHOSPHATE DIBASIC, ANHYDROUSActive2011-07-05
  • POTASSIUM SULFATEActive2009-10-05
  • MAGNESIUM LACTATE DIHYDRATEActive2007-09-14
  • SODIUM SULFATE ANHYDROUSActive2004-09-08

Showing 15 of 25 Drug Master Files.

FDA compliance signals

1 FDA enforcement record linked to this company.

  • warning_letter2022-07-18

    FDA Warning Letter (drug product)

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