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Methadone Hydrochloride

NDC 0054-3553 · HUMAN PRESCRIPTION DRUG · CONCENTRATE

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA089897
Dosage form / routeCONCENTRATE · ORAL
Active ingredientsMETHADONE HYDROCHLORIDE (10 mg/mL)
Marketing started19880906
Package count1

External sources

Source: openFDA. Public-domain (CC0).