Potassium Clavulanate and Microcrystalline Cellulose 1:1 ROW

Formulation:
A powder mixture of Potassium Clavulanate and extra dry microcrystalline cellulose in a 1:1 weight ratio.

Therapeutical Category:
The combination of clavulanic acid and amoxicillin can be used against a variety of Beta-lactamase producing Gram positive and Gram negative bacteria. Clavulanic acid enhances the activity of amoxicillin as a broad spectrum antibiotic because of its powerful inhibitory effect on many Beta-lactamase enzymes. Clavulanic acid itself has little useful therapeutic activity.

Application:
The product is suitable for the manufacture of tablets after addition of appropriate excipients and amoxicillin.

Not suitable for sales to the USA market.

Appearance:
White or almost white powder, hygroscopic.

Identification of potassium clavulanate (HLPC):
Positive.

Identification of cellulose:
Positive.

Assay clavulanic acid (on dry basis):
35.9 to 45.0%.

Assay potassium clavulanate (on dry basis):
42.8 to 53.6%.

pH (1%):
4.8 to 8.0.

Water:
≤ 2.5%.

Related substances: total *:
≤ 1.0%.

Bulk density:
≤ 0.60 g/ml.

Tapped density:
≤ 0.85 g/ml.

Shelf life:
5 years.

Storage:
In an airtight container, at a temperature below 15º Celsius.

Remark:
Meets the requirements of the latest edition of USP.

* Related substances relative to the blend