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Methadone Hydrochloride

NDC 17856-0392 · HUMAN PRESCRIPTION DRUG · CONCENTRATE

Labeler / ManufacturerATLANTIC BIOLOGICALS CORP.
Marketing categoryAbbreviated NDA (generic) · App ANDA040180
Dosage form / routeCONCENTRATE · ORAL
Active ingredientsMETHADONE HYDROCHLORIDE (10 mg/mL)
Marketing started20190514
Package count6

External sources

Source: openFDA. Public-domain (CC0).