| NDC Code: |
0555-9009 |
| Proprietary Name: |
Nortrel |
| Suffix: |
(21 Day Regimen) |
| Non-Proprietary Name: |
Norethindrone and Ethinyl Estradiol |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
13-06-2001 |
| Category Name: |
ANDA |
| Application Number: |
ANDA072693 |
| Labeler: |
BARR LABORATORIES INC. |
| Substance Name: |
ETHINYL ESTRADIOL; NORETHINDRONE |
| Active Numerator Strength: |
.035; 1 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
| DEA Schedule: |
|
