Low Outlier
Strength
50 mg/1
Manufacturer
Precision Dose Inc.NDC
68094085362
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
2/19/2025
Active Ingredients
NALTREXONE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA075274On Market Since
10/29/2014
Pharmacological Classes
Opioid Antagonist
Opioid Antagonists
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