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Aminolevulinic Acid Hydrochloride USP Related Compound B is chemically Methyl 5-(1,3-dioxoisoindolin-2-yl)-4-oxopentanoate (as per USP).
Aminolevulinic Acid Hydrochloride USP Related Compound B is supplied with detailed characterization data compliant with regulatory guideline. Aminolevulinic Acid Hydrochloride USP Related Compound B 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 Aminolevulinic Acid Hydrochloride.

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.

Norgestimate 5-ene Analog (USP) is chemically Mixture of (E) and (Z)-13-Ethyl-17β-acetoxy-18,19-dinor-17α-pregn-5-en-20-yn-3-one oxime (as per USP). Norgestimate 5-ene Analog (USP) is supplied with detailed characterization data compliant with regulatory guideline. Norgestimate 5-ene Analog (USP) 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 Norgestimate.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.

Glycinexylidide (TFA Salt) is chemically 2-Amino-N-(2,6-dimethylphenyl)acetamide 2,2,2-trifluoroacetate.
Glycinexylidide (TFA Salt) is supplied with detailed characterization data compliant with regulatory guideline. Glycinexylidide (TFA 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 Ranolazine.

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.

Diltiazem EP Impurity D is chemically (2S,3S)-5-[2-(Methylamino)ethyl]-2-(4-methoxyphenyl)-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepin-3-yl acetate HCl ; .
It is also known as N-Desmethyl Diltiazem Hydrochloride ; .
Diltiazem EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Diltiazem EP Impurity D 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 Diltiazem.

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.

Fluticasone Propionate EP Impurity A is chemically 6α,9-Difluoro-11β-hydroxy-16α-methyl-3-oxo-17-(propanoyloxy) androsta-1,4-diene-17β-carboxylic acid ;.
It is also known as Fluticasone EP Impurity A ; Fluticasone Carboxylic Acid Propionate ; .
Fluticasone Propionate EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Fluticasone Propionate EP Impurity A 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 Fluticasone.

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.

Mycophenolate Mofetil Impurity 1 is chemically 5,7-dihydroxy-4-methylisobenzofuran-1(3H)-one.
Mycophenolate Mofetil Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Mycophenolate Mofetil Impurity 1 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 Mycophenolate Mofetil.

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.

Diltiazem DTZ-I Impurity is chemically (2S,3S)-2-(4-Methoxyphenyl)-5-methyl-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]thiazepin-3-yl acetate.
Diltiazem DTZ-I Impurity is supplied with detailed characterization data compliant with regulatory guideline. Diltiazem DTZ-I Impurity 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 Diltiazem.

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.