- Minimum Order Quantity :
- Unit of Measure :
- Formulations Type :
- General Drugs
- Formulations Form :
- Gender/Age Group :
- Suitable For All Ages
- Storage Instructions :
- Store in Cool
Generic Premarin Tablets
Premarin for oral administration contains a mixture of conjugated estrogens obtained exclusively from natural sources, occurring as the sodium salts of water-soluble estrogen sulfates blended to represent the average composition of material derived from pregnant mares' urine. It is a mixture of sodium estrone sulfate and sodium equilin sulfate. It contains as concomitant components, as sodium sulfate conjugates, 17ÃÅ½ÃÂ±-dihydroequilin, 17ÃÅ½ÃÂ±-estradiol, and 17ÃÅ½ÃÂ²-dihydroequilin. Tablets for oral administration are available in 0.3 mg, 0.45 mg, 0.625 mg, 0.9 mg, and 1.25 mg strengths of conjugated estrogens.
Premarin 0.3 mg, 0.45 mg, 0.625 mg, 0.9 mg, and 1.25 mg tablets also contain the following inactive ingredients: calcium phosphate tribasic, carnauba wax, hydroxypropyl cellulose, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, powdered cellulose, sucrose, and titanium dioxide.
- 0.3 mg tablets also contain: D&C Yellow No. 10 and FD&C Blue No. 2.
- 0.45 mg tablets also contain: FD&C Blue No. 2.
- 0.625 mg tablets also contain: FD&C Blue No. 2 and FD&C Red No. 40.
- 0.9 mg tablets also contain: D&C Red No. 30 and D&C Red No. 7.
- 1.25 mg tablets also contain: black iron oxide, D&C Yellow No. 10 and FD&C Yellow No. 6.
Premarin tablets comply with USP Dissolution Test criteria as outlined below:
|Premarin 1.25 mg tablets||USP Dissolution Test 4|
|Premarin 0.3 mg, 0.45 mg and 0.625 mg tablets||USP Dissolution Test 5|
|Premarin 0.9 mg tablets||USP Dissolution Test 6|
H. O.-102, Sector-78, Sakatpur, Gurgaon, Haryana, 122002, India