FDA NDC
Inluriyo
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 0002-1717
- Proprietary name
- Inluriyo
- Nonproprietary name
- imlunestrant
- Labeler
- Eli Lilly and Company
- Dosage form
- TABLET, FILM COATED
- Strength
- 200 mg/1
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