Procedure for Assay and Stability Determination of Idoxuridine

Simpson, Charles A.; Zappala, Alfred F.

doi:10.1002/jps.2600531015

Search citation statements

Order By: Relevance

Paper Sections

Select...

Alkaloids Both Macek1

Citation Types

Supporting

Mentioning

Contrasting

Year Published

1966

1993

Publication Types

Select...

Article5

Relationship

Self Cite0

Independent5

Authors

Journals

Cited by 5 publications

(1 citation statement)

References 7 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Applications of chromatography in general (1854), of column partition chromatography (1152), of PC (1092), and of TLC (333,741,1153,2311) to pharmaceutical analysis have been reviewed. Column chromatography has been used for the isolation and analysis of phenothiazine (814), glyceryl trinitrate (810), phenobarbital (1028), picrotoxin (892), and idoxuridine (1881).…”

Section: Alkaloids Both Macekmentioning

confidence: 99%

Chromatography

Heftmanń¹

1966

Anal. Chem.

View full text Add to dashboard Cite

Section: Alkaloids Both Macekmentioning

confidence: 99%

Chromatography

Heftmanń¹

1966

Anal. Chem.

View full text Add to dashboard Cite

Qualitative and Quantitative Tests for Idoxuridine

1966

Journal of Pharmaceutical Sciences

View full text Add to dashboard Cite

Provisional, unofficial monographs are developed by the Drug Standards Laboratory, in cooperation with the manufacturers of the drug concerned, for publication in the Journal of Pbarmaceutical Sciences. The ready availability of this information affords discriminating medical and pharmaceutical practitioners with an added basis for confidence in the quality of new drug products generally, and of those covered by the monographs particularly. Such monographs will appear on drugs representing new chemical entities for which suitable identity tests and assay procedures are not available in the published literature. The purity and assay limits reported for the drugs and their dosage forms are based on observations made on samples representative of commercial production and are considered to be reasonable within expected analytical and manufacturing variation.

show abstract