DIVIGEL

This brand name is authorized in Canada, Estonia, Finland, Ireland, Japan, Lithuania, Poland, Singapore, United States

Active ingredients

The drug DIVIGEL contains one active pharmaceutical ingredient (API):

1 Estradiol UNII 4TI98Z838E - ESTRADIOL

Estradiol, is chemically and biologically identical to endogenous human estradiol. It substitutes for the loss of oestrogen production in menopausal women, and alleviates menopausal symptoms. Oestrogens prevent bone loss following menopause or ovariectomy. Read about Estradiol

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
DIVIGEL Gel	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
G03CA03	Estradiol	G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03C Estrogens → G03CA Natural and semisynthetic estrogens, plain
Discover more medicines within G03CA03

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country	Identification scheme	Identifier(s)
Country: CA	Health Products and Food Branch	Identifier(s): 02424835, 02424843, 02424924
Country: EE	Ravimiamet	Identifier(s): 1030510, 1063415, 1741980
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 565473, 565499
Country: IE	Health Products Regulatory Authority	Identifier(s): 21272
Country: JP	医薬品医療機器総合機構	Identifier(s): 2473700M1020
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1002575, 1002576
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100089913, 100089920, 100409329, 100443295
Country: SG	Health Sciences Authority	Identifier(s): 11642P, 11644P
Country: US	FDA, National Drug Code	Identifier(s): 68025-065, 68025-066, 68025-067, 68025-083, 68025-086