Femring - 0430-6202-40 - (estradiol acetate)

Alphabetical Index


Drug Information of Femring

Product NDC: 0430-6202
Proprietary Name: Femring
Non Proprietary Name: estradiol acetate
Active Ingredient(s): .1    mg/d & nbsp;   estradiol acetate
Administration Route(s): VAGINAL
Dosage Form(s): RING
Coding System: National Drug Codes(NDC)

Labeler Information of Femring

Product NDC: 0430-6202
Labeler Name: Warner Chilcott (US), LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021367
Marketing Category: NDA
Start Marketing Date: 20030701

Package Information of Femring

Package NDC: 0430-6202-40
Package Description: 12 CARTON in 1 CASE (0430-6202-40) > 1 POUCH in 1 CARTON > 90 d in 1 POUCH

NDC Information of Femring

NDC Code 0430-6202-40
Proprietary Name Femring
Package Description 12 CARTON in 1 CASE (0430-6202-40) > 1 POUCH in 1 CARTON > 90 d in 1 POUCH
Product NDC 0430-6202
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name estradiol acetate
Dosage Form Name RING
Route Name VAGINAL
Start Marketing Date 20030701
Marketing Category Name NDA
Labeler Name Warner Chilcott (US), LLC
Substance Name ESTRADIOL ACETATE
Strength Number .1
Strength Unit mg/d
Pharmaceutical Classes Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA]

Complete Information of Femring


General Information