Strength
50 mg/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
47335032683
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
NALTREXONE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA090356On Market Since
2/29/2012
Pharmacological Classes
Opioid Antagonist
Opioid Antagonists
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