Estradiol / Norethindrone Acetate 1 mg/1
Estradiol and Norethindrone Acetate · TABLET, FILM COATED · Breckenridge Pharmaceutical, Inc.
This is a prescription tablet that combines estrogen and progestin hormones and is used to treat symptoms of menopause such as hot flashes and vaginal dryness. It may also be prescribed to prevent bone loss in postmenopausal women.
Key Facts
- Brand Name
- Estradiol / Norethindrone Acetate
- Generic Name
- Estradiol and Norethindrone Acetate
- NDC Code (Product)
51991-474- Manufacturer
- Breckenridge Pharmaceutical, Inc.
- Strength
- 1 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA078324
- Drug Class
- Estrogen [EPC]
- Marketing Start
- 04/17/2008
Recall History
No Recall HistoryFrequently Asked Questions
What is Estradiol / Norethindrone Acetate used for?
This is a prescription tablet that combines estrogen and progestin hormones and is used to treat symptoms of menopause such as hot flashes and vaginal dryness. It may also be prescribed to prevent bone loss in postmenopausal women.
Is Estradiol / Norethindrone Acetate a controlled substance?
Estradiol / Norethindrone Acetate is not classified as a controlled substance by the DEA.
What is the generic name for Estradiol / Norethindrone Acetate?
The generic name for Estradiol / Norethindrone Acetate is Estradiol and Norethindrone Acetate. There are 8 other brand versions of Estradiol and Norethindrone Acetate.
What is the NDC code for Estradiol / Norethindrone Acetate 1 mg/1?
The NDC (National Drug Code) for Estradiol / Norethindrone Acetate 1 mg/1 is 51991-474, listed by Breckenridge Pharmaceutical, Inc..