Some documents for this product are not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain them. Send request. ×

Active ingredient:

DIHYDRÁT SODNÉ SOLI IBUPROFENU (IBUPROFENUM NATRICUM DIHYDRICUM)

Available from:

Reckitt Benckiser Healthcare International Ltd., Slough

ATC code:

M01AE01

Dosage:

256MG

Pharmaceutical form:

Obalená tableta

Administration route:

Perorální podání

Units in package:

4 III, Blistr

Prescription type:

Volně prodejné léčivé přípravky

Authorization status:

B - přípravek po provedené změně.

Authorization number:

07/ 812/10-C

Authorization date:

2011-12-31