|
Information For:
|
Revisions to USP32–NF27, Second Supplement
Published April 2009
General Chapters
Monographs:
A–C
D–N
O–S
T–Z
| Monograph Title
|
Monograph Section
|
Scientific Liaison
|
| <1> INJECTIONS PF 34(4) Pg. 1020 |
INGREDIENTS |
Desmond Hunt |
| <11> USP REFERENCE STANDARDS PF 34(4) Pg. 1021 |
USP Cloprostenol Sodium RS, USP Dextroamphetamine Related
Compound A RS, USP Dextroamphetamine Related Compound B RS, USP Enrofloxacin
RS, USP Enrofloxacin Related Compound Mixture RS, USP N-Ethylpiperazine RS,
USP Granisetron Related Compound C RS, USP Granisetron Related Compound D RS,
USP Purified Guggul Extract RS, USP Guggulsterone Z RS, USP Itraconazole RS,
USP Oxaliplatin RS, USP Oxaliplatin Related Compound A RS, USP Oxaliplatin
Related Compound B RS, USP Oxaliplatin Related Compound C RS, USP Oxaliplatin
Related Compound D RS, USP Guanine RS., USP Silicified Microcrystalline
Cellulose RS, USP Ecamsule Solution RS, USP Ecamsule Triethanolamine RS, USP
Ecamsule Related Compound A RS, USP Ecamsule Related Compound B RS, USP
Ecamsule Related Compound C RS, USP Ecamsule Related Compound D RS, USP
Ecamsule Related Compound E RS, USP Ecamsule Related Compound F RS, USP
Ecamsule Related Compound G RS, USP Ethyl Maltol RS, USP Mesna RS, USP Mesna
Related Compound A RS, USP Mesna Related Compound B RS, USP Moxifloxacin
Hydrochloride RS, USP Moxifloxacin Related Compound A RS, USP Behenoyl
Polyoxylglycerides RS, USP Risedronate Sodium RS, USP Risedronate Related
Compound A RS, USP Risedronate Related Compound B RS, USP Risedronate Related
Compound C RS, USP Tramadol Hydrochloride RS, USP Tramadol Related Compound A
RS |
Elena Gonikberg |
| <207> TEST FOR 1,6-ANHYDRO DERIVATIVE FOR ENOXAPARIN
SODIUM PF 34(1) Pg. 143 |
Title, Introduction, INTRODUCTION, DEPOLYMERIZATION OF
ENOXAPARIN SODIUM BY HEPARINASES AND RESULTING OLIGOSACCHARIDES, PROCEDURE,
APPENDIX 1, APPENDIX 2 |
Anita Szajek |
| <467> RESIDUAL SOLVENTS PF 34(5) Pg. 1232 |
OTHER ANALYTICAL PROCEDURES |
Horacio Pappa |
| <621> CHROMATOGRAPHY PF 34(1) Pg. 152 |
Stationary Phase, Flow Rate(GC), and Flow Rate (HPLC) of the
SYSTEM SUITABILITY section |
Horacio Pappa |
| <643> TOTAL ORGANIC CARBON PF 33(4) Pg. 720 |
Introduction, APPARATUS REQUIREMENTS, CONTAINER PREPARATION,
STANDARD SOLUTION, TEST SOLUTION, OTHER CONTROL SOLUTIONS, SYSTEM
SUITABILITY, PROCEDURE, GLASSWARE PREPARATION-CONTAINER PREPARATION, WATER
SAMPLE |
Antonio Hernandez-Cardoso |
| <711> DISSOLUTION PF 34(5) Pg. 1243 |
USP REFERENCE STANDARDS <11>, APPARATUS |
William Brown |
| <785> OSMOLALITY AND OSMOLARITY PF 34(1) Pg. 157 |
MEASUREMENT OF OSMOLALITY |
Horacio Pappa |
| <891> THERMAL ANALYSIS PF 34(4) Pg. 1023 |
INTRODUCTION, TRANSITION TEMPERATUREAND MELTING POINT
TEMPERATURES, DETERMINATION OF TRANSITION TEMPERATURE (MELT ONSET
TEMPERATURE) AND MELTING POINT TEMPERATURE, THERMOGRAVIMETRIC ANALYSIS,
HOT-STAGE MICROSCOPY, EUTECTIC IMPURITY ANALYSIS |
Antonio Hernandez-Cardoso |
| <905> UNIFORMITY OF DOSAGE UNITS PF 34(5) Pg. 1290 |
Introduction, CONTENT UNIFORMITY, WEIGHT VARIATION, CRITERIA |
William Brown |
| <1090> IN VIVO BIOEQUIVALENCE GUIDANCES PF 34(4) Pg. 1028 |
Title, Introduction, DRUG PROTOCOL CONTENTS, GENERAL GUIDANCES,
BACKGROUND, BIOAVAILABILITY, BIOEQUIVALENCE, AND DISSOLUTION, DISSOLUTION AND
IN VITRO PRODUCT PERFORMANCE, BIOWAIVER, APPENDIX |
William Brown |
General Chapters
Monographs:
A–C
D–N
O–S
T–Z
|
|