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1,2-Dihydro Diethyl Loteprednol Carbonate is chemically (8S,9S,10R,11S,13S,14S,17R)-17-((ethoxycarbonyl)oxy)-11-hydroxy-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-17-carboxylic (ethyl carbonic) anhydride.
1,2-Dihydro Diethyl Loteprednol Carbonate is supplied with detailed characterization data compliant with regulatory guideline. 1,2-Dihydro Diethyl Loteprednol Carbonate can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Loteprednol.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ISP Standards products are for analytical purpose only and not for human use.

Desmethyl Fluorometholone is chemically (8S,9R,10S,11S,13S,14S,17R)-17-Acetyl-9-fluoro-11,17-dihydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-3-one.
Desmethyl Fluorometholone is supplied with detailed characterization data compliant with regulatory guideline. Desmethyl Fluorometholone can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Fluorometholone.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ISP Standards products are for analytical purpose only and not for human use.

Bilastine Impurity 20 is chemically Ethyl 2-(1-(ethoxycarbonyl)piperidin-4-yl)-1H-benzo[d]imidazole-1-carboxylate.
Bilastine Impurity 20 is supplied with detailed characterization data compliant with regulatory guideline. Bilastine Impurity 20 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Bilastine.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ISP Standards products are for analytical purpose only and not for human use.

Mefenamic Acid is chemically 2-(2,3-Dimethylanilino)benzoic acid.
Mefenamic Acid is supplied with detailed characterization data compliant with regulatory guideline. Mefenamic Acid can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Mefenamic Acid.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ISP Standards products are for analytical purpose only and not for human use.

(3’S,3R,4S)-Desfluoro Ezetimibe is chemically (3R,4S)-1-(4-Fluorophenyl)-3-((S)-3-hydroxy-3-phenylpropyl)-4-(4-hydroxyphenyl)azetidin-2-one.
(3’S,3R,4S)-Desfluoro Ezetimibe is supplied with detailed characterization data compliant with regulatory guideline. (3’S,3R,4S)-Desfluoro Ezetimibe can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Ezetimibe.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ISP Standards products are for analytical purpose only and not for human use.

Pitavastatin (+)-Phenylethylamine Salt is chemically (R)-1-Phenylethan-1-amine (3R,5S,E)-7-(2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl)-3,5-dihydroxyhept-6-enoate.
Pitavastatin (+)-Phenylethylamine Salt is supplied with detailed characterization data compliant with regulatory guideline. Pitavastatin (+)-Phenylethylamine Salt can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Pitavastatin.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ISP Standards products are for analytical purpose only and not for human use.