FDA NDC
Nortrel 21 Day
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 0555-9009
- Proprietary name
- Nortrel 21 Day
- Nonproprietary name
- Norethindrone and Ethinyl Estradiol
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- TABLET
- Strength
- 1 mg/1
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