AMBIENT AIR;
ARTICLE;
DRUG BIOAVAILABILITY;
DRUG DOSAGE FORM;
DRUG DOSE REGIMEN;
DRUG MANUFACTURE;
DRUG SCREENING;
DRUG SOLUBILITY;
DRUG STABILITY;
DRUG STORAGE;
FIXED DOSE COMBINATION;
HUMIDITY;
IN VITRO STUDY;
PHYSICAL ACTIVITY;
QUALITY CONTROL;
TABLET FORMULATION;
TUBERCULOSIS;
ANTITUBERCULAR AGENTS;
CHEMISTRY, PHARMACEUTICAL;
CHEMISTRY, PHYSICAL;
DRUG COMBINATIONS;
DRUG STABILITY;
DRUG STORAGE;
QUALITY CONTROL;
SOLUBILITY;
TABLETS;
TEMPERATURE;
THERAPEUTIC EQUIVALENCY;
In vitro analysis of rifampicin and its effect on quality control tests of rifampicin containing dosage forms
In Press
Agrawal S, Panchagnula R (2004) In vitro analysis of rifampicin and its effect on quality control tests of rifampicin containing dosage forms. Pharmazie (In Press).
Effects of different types of lactose and disintegrants on dissolution stability of hydrochlorothiazide
Desai DS, Rubitski BA, Bergum JS, Varia SA (1994) Effects of different types of lactose and disintegrants on dissolution stability of hydrochlorothiazide. Int J Pharm 110: 257-265.
The effect of aging on the dissolution of wet granulated tablets containing superdisintegrants
Gordon MS, Rudraraju VS, Rhie JK, Chowhan ZT (1993) The effect of aging on the dissolution of wet granulated tablets containing superdisintegrants. Int J Pharm 97: 119-131.
The international conference on harmonization of technical requirements for registration of pharmaceuticals for human use. Stability testing of new drug substances and products. Q1A(R)
Geneva
ICH (2000) The international conference on harmonization of technical requirements for registration of pharmaceuticals for human use. Stability testing of new drug substances and products. Q1A(R). International Conference on Harmonization, Geneva.
The international conference on harmonization of technical requirements for registration of pharmaceuticals for human use. Evaluation of stability data. Draft consensus guideline
Geneva
ICH (2002a) The international conference on harmonization of technical requirements for registration of pharmaceuticals for human use. Evaluation of stability data. Draft consensus guideline. International Conference on Harmonization, Geneva.
The international conference on harmonization of technical requirements for registration of pharmaceuticals for human use. Stability data package for registration in climatic zone III and IV. Draft consensus guideline
Geneva
ICH (2002b) The international conference on harmonization of technical requirements for registration of pharmaceuticals for human use. Stability data package for registration in climatic zone III and IV. Draft consensus guideline. International Conference on Harmonization, Geneva.
Methods to compare dissolution profiles and a rationale for wide dissolution specifications for metoprolol tartrate tablets
Polli JE, Rekhi GS, Augsburger LL, Shah VP (1997) Methods to compare dissolution profiles and a rationale for wide dissolution specifications for metoprolol tartrate tablets. J Pharm Sci 86: 690-700.
