Formulation Development and Evaluation of Fast Disintegrating Tablets of Salbutamol Sulphate, Cetirizine Hydrochloride in Combined Pharmaceutical Dosage Form: A New Era in Novel Drug Delivery for Pediatrics and Geriatrics

Table 7

Evaluation parameters for Salbutamol Sulphate, Cetirizine Hydrochloride FDT.

Serial; number	Evaluation parameters	Results
1	Weight variation (IP)	Passed
2	Thickness (mm) ± S.D	3.63 ± 0.06
3	Hardness (Kg/cm^2) ± S.D	1.8 ± 0.29
4	Friability (%)	0.3
5	Disintegration time (sec) ± S.D	45 ± 2.34
6	Wetting time (sec) ± S.D	28 ± 1.53
7	Drug content uniformity (mg) ± S.D	SAL-100.8 ± 3.36,; CET-104.7 ± 1.97

Average of three determinations.
Average of six determinations.