FDA NDC
Moexipril Hydrochloride
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 62135-967
- Proprietary name
- Moexipril Hydrochloride
- Nonproprietary name
- Moexipril Hydrochloride
- Labeler
- Chartwell RX, LLC
- Dosage form
- TABLET, FILM COATED
- Strength
- 7.5 mg/1
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