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Last Updated: November 24, 2024

Details for New Drug Application (NDA): 211783

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NDA 211783 describes ESTRADIOL, which is a drug marketed by Alvogen, Mylan, Padagis Israel, Prasco, Teva Pharms Usa, Amneal, Mylan Technologies, Zydus Pharms, Solaris Pharma Corp, Chemo Research Sl, Novitium Pharma, Quagen, Ortho Mcneil Pharm, Barr Labs Inc, Dr Reddys Labs Sa, Epic Pharma Llc, Lannett Co Inc, Norvium Bioscience, Usl Pharma, Amneal Pharms, Aurobindo Pharma, Glenmark Pharms Ltd, Barr, Breckenridge Pharm, Naari Pte Ltd, Novast Labs, Xiromed, Dr Reddys, Am Regent, Fosun Pharma, Hikma, and Watson Labs, and is included in forty-seven NDAs. It is available from thirty-six suppliers. Additional details are available on the ESTRADIOL profile page.

The generic ingredient in ESTRADIOL is estradiol valerate. There are seventy-five drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the estradiol valerate profile page.

Summary for 211783

Tradename:	ESTRADIOL
Applicant:	Chemo Research Sl
Ingredient:	estradiol
Patents:	0

Pharmacology for NDA: 211783

Mechanism of Action	Estrogen Receptor Agonists

Medical Subject Heading (MeSH) Categories for 211783

Estrogens

Suppliers and Packaging for NDA: 211783

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
ESTRADIOL	estradiol	GEL;TRANSDERMAL	211783	ANDA	Xiromed, LLC	70700-143	70700-143-35	30 PACKET in 1 CARTON (70700-143-35) / .25 g in 1 PACKET
ESTRADIOL	estradiol	GEL;TRANSDERMAL	211783	ANDA	Xiromed, LLC	70700-144	70700-144-35	30 PACKET in 1 CARTON (70700-144-35) / .5 g in 1 PACKET

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	GEL;TRANSDERMAL			Strength	0.1% (0.25GM/PACKET)
Approval Date:	Aug 10, 2022	TE:	AB	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	GEL;TRANSDERMAL			Strength	0.1% (0.5GM/PACKET)
Approval Date:	Aug 10, 2022	TE:	AB	RLD:	No

Profile for product number 003

Active Rx/OTC/Discontinued:	RX	Dosage:	GEL;TRANSDERMAL			Strength	0.1% (1GM/PACKET)
Approval Date:	Aug 10, 2022	TE:	AB	RLD:	No

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