Evaluation of the functional equivalence of Crospovidone NF from different sources. II. Standard performance test

Pharmaceutical Development and Technology

Volumn 6, Issue 3, 2001, Pages 419-430

  Shah, Umang ^a   Augsburger, Larry ^b  

^a PFIZER GLOBAL RESEARCH AND DEVELOPMENT   (United States)

^b UNIVERSITY OF MARYLAND SCHOOL OF PHARMACY   (United States)

Author keywords

Crospovidone NF; Disintegration force; Liquid uptake; Multiple suppliers; Settling volume; Standard performance test

Indexed keywords

CROSPOVIDONE;

ARTICLE; DISSOLUTION; DRUG FORMULATION; DRUG MANUFACTURE; MORPHOLOGY; PARTICLE SIZE; PERFORMANCE; POROSITY; PRIORITY JOURNAL;

BIOLOGICAL AVAILABILITY; CARBOXYMETHYLCELLULOSE; DRUG EVALUATION, PRECLINICAL; MICROSCOPY, ELECTRON, SCANNING; PHARMACEUTIC AIDS; POROSITY; POVIDONE; REFERENCE STANDARDS; SOLUBILITY; THERMOGRAVIMETRY;

EID: 0034928227     PISSN: 10837450     EISSN: None     Source Type: Journal    
DOI: 10.1081/PDT-100002250     Document Type: Article

References (20)

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4. Effect of molecular structure variation on the disintegrant action of sodium starch glycolate
5. A new tablet disintegrating agent: Cross-linked polyvinylpyrrolidone
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17. Tablet water uptake and disintegrating force measurements