Junel 21 Day 20 ug/1
Norethindrone Acetate and Ethinyl Estradiol · TABLET · Teva Pharmaceuticals USA, Inc.
Junel 21 Day is a tablet containing norethindrone acetate and ethinyl estradiol at 20 ug/1, taken oral. Manufactured by Teva Pharmaceuticals USA, Inc..
Key Facts
- Brand Name
- Junel 21 Day
- Generic Name
- Norethindrone Acetate and Ethinyl Estradiol
- NDC Code (Product)
0555-9025- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- Strength
- 20 ug/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA076380
- Drug Class
- Estrogen [EPC]
- Marketing Start
- 09/18/2003
Recall History
No Recall HistoryFrequently Asked Questions
What is Junel 21 Day used for?
Junel 21 Day contains Norethindrone Acetate and Ethinyl Estradiol. It is a tablet taken oral. Consult your doctor for specific uses.
Is Junel 21 Day a controlled substance?
Junel 21 Day is not classified as a controlled substance by the DEA.
What is the generic name for Junel 21 Day?
The generic name for Junel 21 Day is Norethindrone Acetate and Ethinyl Estradiol. There are 12 other brand versions of Norethindrone Acetate and Ethinyl Estradiol.
What is the NDC code for Junel 21 Day 20 ug/1?
The NDC (National Drug Code) for Junel 21 Day 20 ug/1 is 0555-9025, listed by Teva Pharmaceuticals USA, Inc..
Other Norethindrone Brands
See all →- Jinteli5 ug/10093-3122
- LO LOESTRIN FE50090-1456
- Aurovela Fe 1/2065862-940
- Hailey 1.5/30.03 mg/168462-504
- NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE0378-7303
- Norethindrone Acetate and Ethinyl Estradiol.005 mg/175834-130
- Aurovela 1.5/3030 ug/165862-935
- Hailey Fe 1.5/3068462-503
- Norethindrone Acetate and Ethinyl Estradiol, and Ferrous Fumarate69238-1686
- Junel Fe 240093-5328
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)