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Methadone Hydrochloride

NDC 81298-7500 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerLong Grove Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208306
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsMETHADONE HYDROCHLORIDE (200 mg/20mL)
Marketing started20250628
Package count1

External sources

Source: openFDA. Public-domain (CC0).