FDA NDC Directory · JSON-LD · Markdown

Methamphetamine Hydrochloride

NDC 68308-115 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameMETHAMPHETAMINE HYDROCHLORIDE
Labeler / ManufacturerMayne Pharma Commercial LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091189
Dosage form / routeTABLET · ORAL
Active ingredientsMETHAMPHETAMINE HYDROCHLORIDE (5 mg/1)
Marketing started20100426
Package count1

External sources

Source: openFDA. Public-domain (CC0).