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CIPLA DAPAGLIFLOZIN; DAPAGLICIP; FOCIPRA (Cipla Australia Pty Ltd)

Product name
CIPLA DAPAGLIFLOZIN; DAPAGLICIP; FOCIPRA
Date registered
Evaluation commenced
Decision date
Approval time
130 (255 working days)
Active ingredients
dapagliflozin (as propanediol monohydrate)
Registration type
New generic medicine
Indication
Type 2 diabetes mellitus
Glycaemic control

CIPLA DAPAGLIFLOZIN; DAPAGLICIP; FOCIPRA (film-coated tablet) is indicated in adults with type 2 diabetes mellitus:

  • as monotherapy as an adjunct to diet and exercise in patients for whom metformin is otherwise indicated but was not tolerated.
  • as initial combination therapy with metformin, as an adjunct to diet and exercise, to improve glycaemic control when diet and exercise have failed to provide adequate glycaemic control and there are poor prospects for response to metformin monotherapy(for example, high initial haemoglobin A1c [HbA1c] levels).
  • in combination with other anti-hyperglycaemic agents to improve glycaemic control, when these together with diet and exercise, do not provide adequate glycaemic control (see section 5.1 Pharmacodynamic properties - clinical trials and section 4.4 Special warnings and precautions for use for available data on different add-on combination therapies).
Prevention of hospitalisation for heart failure

CIPLA DAPAGLIFLOZIN; DAPAGLICIP; FOCIPRA is indicated in adults with type 2 diabetes mellitus and established cardiovascular disease or risk factors for cardiovascular disease to reduce the risk of hospitalization for heart failure (see section 5.1 Pharmacodynamic properties - clinical trials).

Heart failure

CIPLA DAPAGLIFLOZIN; DAPAGLICIP; FOCIPRA is indicated in adults for the treatment of symptomatic heart failure with reduced ejection fraction, as an adjunct to standard of care therapy (see section 5.1 Pharmacodynamic properties).

Chronic kidney disease

CIPLA DAPAGLIFLOZIN; DAPAGLICIP; FOCIPRA is indicated to reduce the risk of progressive decline in kidney function in adults with proteinuric chronic kidney disease (CKD Stage 2, 3 or 4 and urine ACR ≥30 mg/g)

Registration process

First generic
First approval of a medicine that contains the same active ingredient as and is bioequivalent to an existing medicine

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