Nortrel 21 Day .035 mg/1
Norethindrone and Ethinyl Estradiol · TABLET · Teva Pharmaceuticals USA, Inc.
No Recall History
Plain English
Nortrel 21 Day is a tablet containing norethindrone and ethinyl estradiol at .035 mg/1, taken oral. Manufactured by Teva Pharmaceuticals USA, Inc..
Key Facts
- Brand Name
- Nortrel 21 Day
- Generic Name
- Norethindrone and Ethinyl Estradiol
- NDC Code (Product)
0555-9009- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- Strength
- .035 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA072693
- Drug Class
- Estrogen [EPC]; Progestin [EPC]
- Marketing Start
- 06/13/2001
Recall History
No Recall HistoryFrequently Asked Questions
What is Nortrel 21 Day used for?
Nortrel 21 Day contains Norethindrone and Ethinyl Estradiol. It is a tablet taken oral. Consult your doctor for specific uses.
Is Nortrel 21 Day a controlled substance?
Nortrel 21 Day is not classified as a controlled substance by the DEA.
What is the generic name for Nortrel 21 Day?
The generic name for Nortrel 21 Day is Norethindrone and Ethinyl Estradiol. There are 11 other brand versions of Norethindrone and Ethinyl Estradiol.
What is the NDC code for Nortrel 21 Day .035 mg/1?
The NDC (National Drug Code) for Nortrel 21 Day .035 mg/1 is 0555-9009, listed by Teva Pharmaceuticals USA, Inc..