FDA
Moexipril Hydrochloride
The FDA lists this product in 8 strengths and forms.
Composition
- Active ingredients
- MOEXIPRIL HYDROCHLORIDE 7.5MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- MOEXIPRIL HYDROCHLORIDE 7.5MG · TabletANDA090416-001 · Prescription
- MOEXIPRIL HYDROCHLORIDE 15MG · TabletANDA090416-002 · Prescription
- MOEXIPRIL HYDROCHLORIDE 7.5MG · TabletANDA076204-001 · Prescription
- MOEXIPRIL HYDROCHLORIDE 15MG · TabletANDA076204-002 · Prescription
- MOEXIPRIL HYDROCHLORIDE 7.5MG · TabletThis page
- MOEXIPRIL HYDROCHLORIDE 15MG · TabletANDA078454-002 · Discontinued
- MOEXIPRIL HYDROCHLORIDE 15MG · TabletANDA077536-002 · Prescription
- MOEXIPRIL HYDROCHLORIDE 7.5MG · TabletANDA077536-001 · Prescription
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA078454.
At a glance
- Brand name
- Moexipril Hydrochloride
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Apotex Inc
- Status
- Discontinued
- FDA approval
- 2 Jun 2008
- Application
- ANDA078454-001