Package Label-principal Display Panel (200 mg/28.5 mg* per 5 mL (50 mL Bottle Label))
This is a prescription drug with the NDC number 65862-533-50. It is Amoxicillin and Clavulanate Potassium, which should be taken orally in suspension form. Once reconstituted, the suspension contains 200 mg of Amoxicillin USP as the trihydrate and 28.5 mg of Clavulanic acid as the clavulanate potassium. It is available in a 50 mL bottle. The directions for mixing are given on the label. The usual dosage is every 12 hours, and it must be refrigerated after opening. The drug should be discarded after 10 days, and the inner seal must be intact for use. It is distributed by Aurobindo Pharma USA, Inc, and made in India.*