| Other products |
Alendon ®
(
Alendronate Sodium Tablet )
Alendon? is a preparation of Alendronic acid, a biphosphonate, used in the treatment and prevention of osteoporosis in post-menopausal women. |
 |
Anustat ®
(
Cinchocaine ,Hydrocortisone BP,Neomycine sulphate USP,Esculin sesquihydrate Ointment )
Anustat? is a pale yellow coloured homogenous ointment indicated in Internal and external haemorrhoid ,annal fissure,anal pruritus, perianal eczema, proctitis, pre-operative and post operative treatment of haemorrhoidectomy, post-partum haemorrhoidal condition and as prophylaxis in between attacks. |
 |
Cerivin ®
(
Vinpocetine Tablet )
Cerivin? is indicated in all form of acute & chronic cerebral circulatory insufficiency ,TIA,reversible ischemic neurological deficiency,progressive stroke,completed stroke,post apoleptic conditions,multi -infarct dementia,cerebral atherosclerosis,post traumatic cerebral insufficiency. |
 |
Fertil ®
(
Clomiphene Citrate Tablet )
Fertil? is an ovulatory stimulant which is indicated for the treatment of ovulatory dysfunction in women desiring pregnancy.Clomiphene citrate is indicated for the treatment of ovulatory failure in women desiring pregnancy whose partners are fertile and potent. |
 |
Prosfin ®
(
Finasteride Tablet )
Prosfin? is a preparation of Finasteride which is indicated for the treatment and control of benign prostatic hyperplasia (BPH) to cause regression of the enlarged prostate, to improve urinary flow, and to improve the symptoms associated with BPH.
The development of the prostate gland and subsequent BPH is dependent upon conversion of testosterone to dihydrotestosterone (DHT) within the prostate. Prosfin? belongs to a new class of specific inhibitors of 5a-reductase, an intracellular enzyme which metabolizes testosterone into the more potent androgen, DHT. Finasteride has no affinity for the androgen receptor. |
 |
Recur ®
(
Finasteride coated Tablet )
Recur? is a preparation of Finasteride, a competitive inhibitor of steroid Type II 5a-reductase, an intracellular enzyme that converts the androgen testosterone into 5a-dihydrotestosterone (DHT).
Finasteride is a competitive and specific inhibitor of Type II 5a-reductase, an intracellular enzyme that converts the androgen testosterone into DHT. Finasteride has no affinity for the androgen receptor and has no androgenic or antiandrogenic effects. Inhibition of Type II 5a-reductase blocks the conversion of testosterone to DHT, resulting in significant decreases in serum and tissue DHT concentrations. In men with male pattern hair loss, the balding scalp contains miniaturized hair follicles and increased amounts of DHT compared with hairy scalp. Administration of Finasteride decreases scalp and serum DHT concentrations in these men.Recur? is indicated for the treatment of male pattern hair loss (androgenic alopecia) in male patient only. |
 |
Tamona ®
(
Tamoxifen Tablet )
Tamona? (Tamoxifen) is a non-steroidal, triphenylene-based antineoplastic drug . In breast cancer patients, at the tumour level, Tamoxifen acts primarily as an antioestrogen, preventing oestrogen binding to the oestrogen receptor. If used to the right pa |
 |
Uroflo ®
(
Tamsulosin modified release Capsule )
Uroflo? is indicated for Lower Urinary Tract Symptoms (LUTS), which are common in older men and usually associated with BPH (Benign Prostatic Hyperplasia). Tamsulosin, an alpha one adrenoreceptor antagonist can be considered as an effective and safe first-line treatment option for LUTs. It has superior efficacy over terazosin (very commonly used) both by efficacy and safety. Uroflo has once daily dose and no dose adjustment is required. Patient will get relief from LUTs from the very first dose. |
 |
Vasolax ®
(
Pentoxiphylline Tablet )
Vasolax? (Pentoxifylline) decreases the "stickiness" (viscosity) of blood and thereby improves its flow. This increase blood flow helps patients with peripheral arterial disease to obtain better circulation and oxygen delivery to vital tissues. Vasolax? (Pentoxifylline) is used in patients to treat a condition of painful legs that develop with exercise because of inadequate circulation to the legs and feet (intermittent claudication). |
 |
Zocil ®
(
Cilostazol Tablets )
Zocil? is a preparation of cilostazole. The mechanism of action is to specifically inhibit cellular phosphodiesterase III (PDE III) and suppress cAMP degradation with a resultant increase in cAMP in platelets and blood vessels, leading to inhibition of pla |
 |
Zybex SR ®
(
Bupropion Hydrochloride sustained release Tablet )
Zybex? SR tablets contain bupropion hydrochloride. The exact mechanism of action is not fully understood, but it is believed that it interacts with chemicals called noradrenaline and dopamine in the brain. Zybex? SR is a medicine prescribed by the physicians as a short-term treatment to help stop smoking with appropriate counselling. For many patients, Zybex? SR reduces withdrawal symptoms and the urge to smoke. |
 |
|