LOPREEZA is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Amneal Pharmaceuticals Ny Llc. The primary component is Estradiol; Norethindrone Acetate.
Product ID | 69238-1610_088f747e-f995-4f15-80f4-b72504ffbc36 |
NDC | 69238-1610 |
Product Type | Human Prescription Drug |
Proprietary Name | LOPREEZA |
Generic Name | Estradiol/norethindrone Acetate |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2019-01-07 |
Marketing Category | NDA / NDA |
Application Number | NDA020907 |
Labeler Name | Amneal Pharmaceuticals NY LLC |
Substance Name | ESTRADIOL; NORETHINDRONE ACETATE |
Active Ingredient Strength | 1 mg/1; mg/1 |
Pharm Classes | Estradiol Congeners [CS],Estrogen [EPC],Estrogen Receptor Agonists [MoA],Progesterone Congeners [CS],Progestin [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2019-01-07 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA020907 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2019-01-07 |
Ingredient | Strength |
---|---|
ESTRADIOL | 1 mg/1 |
SPL SET ID: | 966ac064-9eb7-4d15-b271-a7880ed1e79a |
Manufacturer | |
UNII | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
69238-1251 | Lopreeza | estradiol/norethindrone acetate |
69238-1252 | Lopreeza | estradiol/norethindrone acetate |
69238-1609 | LOPREEZA | estradiol/norethindrone acetate |
69238-1610 | LOPREEZA | estradiol/norethindrone acetate |
60846-231 | Activella | Estradiol/norethindrone acetate |
60846-232 | Activella | Estradiol/norethindrone acetate |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LOPREEZA 86321948 4690032 Live/Registered |
Amneal Pharmaceuticals LLC 2014-06-26 |
LOPREEZA 86082169 not registered Dead/Abandoned |
Amneal Pharmaceuticals, LLC 2013-10-03 |