NDC 51991-623
Estradiol / Norethindrone Acetate 0.1 mg / 0.5 mg tablet, film coated
On the label: Breckenridge Pharmaceutical, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pharmaceutics International, Inc. | Hunt Valley, MD, United States | Makes it | Problems found, fixed voluntarilyDec 6, 2024 · 14 inspections |
Product details
- Generic drug
- Estradiol and Norethindrone: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 0.1 mg / 0.5 mg
- Approval
- ANDA ANDA078324
- On the market since
- Jun 9, 2011
- Package NDCs
51991-623-28- Official label
- DailyMed (National Library of Medicine), updated Feb 21, 2024
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