FDA
Naltrexone Hydrochloride
The FDA lists this product in 9 strengths and forms.
Composition
- Active ingredients
- NALTREXONE HYDROCHLORIDE 50MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- NALTREXONE HYDROCHLORIDE 100MG · TabletANDA076264-003 · Prescription
- NALTREXONE HYDROCHLORIDE 25MG · TabletANDA076264-001 · Prescription
- NALTREXONE HYDROCHLORIDE 50MG · TabletANDA076264-002 · Prescription
- NALTREXONE HYDROCHLORIDE 50MG · TabletANDA090356-001 · Prescription
- NALTREXONE HYDROCHLORIDE 50MG · TabletANDA075434-001 · Discontinued
- NALTREXONE HYDROCHLORIDE 50MG · TabletANDA207905-001 · Prescription
- NALTREXONE HYDROCHLORIDE 50MG · TabletANDA075274-001 · Prescription
- NALTREXONE HYDROCHLORIDE 50MG · TabletThis page
- NALTREXONE HYDROCHLORIDE 50MG · TabletANDA091205-001 · Prescription
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA074918.
At a glance
- Brand name
- Naltrexone Hydrochloride
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Barr
- Status
- Prescription
- FDA approval
- 8 May 1998
- Application
- ANDA074918-001