NDC 51285-127-97
Loestrin 21 Day 30 ug/1
Norethindrone Acetate and Ethinyl Estradiol · TABLET
Loestrin 21 Day is an oral contraceptive tablet containing norethindrone acetate and ethinyl estradiol used to prevent pregnancy. It belongs to a class of hormonal birth control medications that combine estrogen and progestin.
Key Facts
- Brand Name
- Loestrin 21 Day
- Generic Name
- Norethindrone Acetate and Ethinyl Estradiol
- NDC Code (Package)
51285-127-97- NDC Code (Product)
51285-127- Manufacturer
- Teva Women's Health LLC
- Strength
- 30 ug/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA076381
- Drug Class
- Estrogen [EPC]
- Marketing Start
- 02/26/2015
Recall History
No Recall HistoryView Full Drug Page
Loestrin 21 Day — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.