This brand name is authorized in United States
The drug PREMPRO contains a combination of these active pharmaceutical ingredients (APIs):
1
Estrogens, conjugated
UNII IU5QR144QX - ESTROGENS, CONJUGATED
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The active ingredients of conjugated estrogens are primarily the sulfate esters of estrone, equilin sulfates, 17α-estradiol and 17β-estradiol. These substitute for the loss of estrogen production in menopausal women, and alleviate menopausal symptoms. Estrogens prevent bone loss following menopause or ovariectomy. |
2
Medroxyprogesterone
UNII C2QI4IOI2G - MEDROXYPROGESTERONE ACETATE
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Medroxyprogesterone acetate exerts anti-oestrogenic, anti-androgenic and antigonadotrophic effects. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
PREMPRO Sugar-coated tablet | FDA, National Drug Code (US) | MPI, US: SPL/PLR |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
G03FB06 | G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03F Progestogens and estrogens in combination → G03FB Progestogens and estrogens, sequential preparations | |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: US | FDA, National Drug Code | Identifier(s): 0046-1105, 0046-1106, 0046-1107, 0046-1108 |
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