Strength
50 mg/1
Manufacturer
Elite Laboratories, Inc.NDC
64850030001
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
NALTREXONE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA075274On Market Since
8/15/2025
Pharmacological Classes
Opioid Antagonist
Opioid Antagonists
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