Estrasorb - 99207-190-01 - (ESTRADIOL HEMIHYDRATE)

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Drug Information of Estrasorb

Product NDC: 99207-190
Proprietary Name: Estrasorb
Non Proprietary Name: ESTRADIOL HEMIHYDRATE
Active Ingredient(s): 2.5    mg/g & nbsp;   ESTRADIOL HEMIHYDRATE
Administration Route(s): TOPICAL
Dosage Form(s): EMULSION
Coding System: National Drug Codes(NDC)

Labeler Information of Estrasorb

Product NDC: 99207-190
Labeler Name: Medicis Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021371
Marketing Category: NDA
Start Marketing Date: 20120222

Package Information of Estrasorb

Package NDC: 99207-190-01
Package Description: 14 POUCH in 1 CARTON (99207-190-01) > 1.74 g in 1 POUCH

NDC Information of Estrasorb

NDC Code 99207-190-01
Proprietary Name Estrasorb
Package Description 14 POUCH in 1 CARTON (99207-190-01) > 1.74 g in 1 POUCH
Product NDC 99207-190
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ESTRADIOL HEMIHYDRATE
Dosage Form Name EMULSION
Route Name TOPICAL
Start Marketing Date 20120222
Marketing Category Name NDA
Labeler Name Medicis Pharmaceutical Corp
Substance Name ESTRADIOL HEMIHYDRATE
Strength Number 2.5
Strength Unit mg/g
Pharmaceutical Classes Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA]

Complete Information of Estrasorb


General Information