Elestrin - 18860-490-02 - (estradiol)

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Drug Information of Elestrin

Product NDC: 18860-490
Proprietary Name: Elestrin
Non Proprietary Name: estradiol
Active Ingredient(s): .6    mg/g & nbsp;   estradiol
Administration Route(s): TRANSDERMAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Elestrin

Product NDC: 18860-490
Labeler Name: Jazz Pharmaceuticals Commercial Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021813
Marketing Category: NDA
Start Marketing Date: 20070601

Package Information of Elestrin

Package NDC: 18860-490-02
Package Description: 1 BOTTLE, PUMP in 1 CARTON (18860-490-02) > 144 g in 1 BOTTLE, PUMP

NDC Information of Elestrin

NDC Code 18860-490-02
Proprietary Name Elestrin
Package Description 1 BOTTLE, PUMP in 1 CARTON (18860-490-02) > 144 g in 1 BOTTLE, PUMP
Product NDC 18860-490
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name estradiol
Dosage Form Name GEL
Route Name TRANSDERMAL
Start Marketing Date 20070601
Marketing Category Name NDA
Labeler Name Jazz Pharmaceuticals Commercial Corp.
Substance Name ESTRADIOL
Strength Number .6
Strength Unit mg/g
Pharmaceutical Classes Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA]

Complete Information of Elestrin


General Information