FDA NDC
Loestrin 21 Day
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 51285-127
- Proprietary name
- Loestrin 21 Day
- Nonproprietary name
- Norethindrone Acetate and Ethinyl Estradiol
- Labeler
- Teva Women's Health LLC
- Dosage form
- TABLET
- Strength
- 1.5 mg/1
HCPCS J8610 Billable units per 11-digit NDC: 180.