PREMPRO

This brand name is authorized in United States

Active ingredients

The drug PREMPRO contains a combination of these active pharmaceutical ingredients (APIs):

1 Estrogens, conjugated
UNII IU5QR144QX - ESTROGENS, CONJUGATED

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.

Read about Estrogens, conjugated
2 Medroxyprogesterone
UNII C2QI4IOI2G - MEDROXYPROGESTERONE ACETATE

Medroxyprogesterone acetate exerts anti-oestrogenic, anti-androgenic and antigonadotrophic effects.

Read about Medroxyprogesterone

Medication package inserts

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

Medicine classification

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
Discover more medicines within G03FB06

Authorization and marketing

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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