# Methamphetamine Hydrochloride

NDC: 68308-115
Generic name: METHAMPHETAMINE HYDROCHLORIDE
Labeler / Manufacturer: Mayne Pharma Commercial LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100426

FDA application: ANDA091189

## Active ingredients

- METHAMPHETAMINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68308-115"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68308-115
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f31f580f-1f08-4a0f-b078-0b9e3308f712