Femring is a Vaginal Ring in the Human Prescription Drug category. It is labeled and distributed by Allergan, Inc.. The primary component is Estradiol Acetate.
Product ID | 0023-5869_b08979c2-5940-48df-b455-d3b2ca68d74d |
NDC | 0023-5869 |
Product Type | Human Prescription Drug |
Proprietary Name | Femring |
Generic Name | Estradiol Acetate |
Dosage Form | Ring |
Route of Administration | VAGINAL |
Marketing Start Date | 2016-05-02 |
Marketing End Date | 2020-05-31 |
Marketing Category | NDA / NDA |
Application Number | NDA021367 |
Labeler Name | Allergan, Inc. |
Substance Name | ESTRADIOL ACETATE |
Active Ingredient Strength | 0 mg/d |
Pharm Classes | Estradiol Congeners [CS],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
NDC Exclude Flag | N |
Marketing Start Date | 2016-05-02 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA021367 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-05-02 |
Marketing End Date | 2020-05-31 |
Ingredient | Strength |
---|---|
ESTRADIOL ACETATE | .1 mg/d |
SPL SET ID: | 9e4c5295-1fe9-4da3-90f9-04204e3e72e4 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0023-5868 | Femring | estradiol acetate |
0023-5869 | Femring | estradiol acetate |
72495-201 | Femring | estradiol acetate |
72495-202 | Femring | estradiol acetate |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() FEMRING 76079677 2740961 Live/Registered |
MILLICENT HOLDINGS, LTD. 2000-06-28 |
![]() FEMRING 74140792 1769635 Dead/Cancelled |
Roussel Uclaf 1991-02-20 |