FDA
Lopressor HCT
The FDA lists this product in 3 strengths and forms.
Composition
- Active ingredients
- HYDROCHLOROTHIAZIDE 50MG; METOPROLOL TARTRATE 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- HYDROCHLOROTHIAZIDE 50MG; METOPROLOL TARTRATE 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletThis page
- HYDROCHLOROTHIAZIDE 25MG; METOPROLOL TARTRATE 50MG · TabletNDA018303-001 · Prescription
- HYDROCHLOROTHIAZIDE 25MG; METOPROLOL TARTRATE 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA018303-002 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA018303.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Lopressor HCT
- Active substance
- hydrochlorothiazide
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Validus Pharms
- Status
- Discontinued
- FDA approval
- 31 Dec 1984
- Application
- NDA018303-003