Forced degradation of ibuprofen in bulk drug and tablets: Determination of specificity, selectivity, and the stability-indicating nature of the USP ibuprofen assay method

Pharmaceutical Technology North America

Volumn 26, Issue 5, 2002, Pages 28-42

  Farmer, Sherri ^a   Anderson, Pamela ^a   Burns, Philip ^a   Velagaleti, Ranga ^a  

^a BASF Corporation   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BIOASSAY; CHEMICAL ANALYSIS; DEGRADATION;

SPECIFICITY;

DRUG PRODUCTS;

IBUPROFEN;

ARTICLE; DRUG DEGRADATION; DRUG STABILITY; EXPOSURE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; OXIDATIVE STRESS; SUNLIGHT; TABLET; TECHNIQUE;

EID: 0036335559     PISSN: 15342131     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Draft revised guidance on Q1A (R) stability testing of new drug substances and products
2. Draft guidance for industry: Analytical procedures and methods validation - Chemistry, manufacturing, and controls documentation
3. Q2A: Text on validation of analytical procedures
4. Ibuprofen and ibuprofen tablets