NDC 0904-7417
Methadone Hydrochloride 10 mg tablet
On the label: Major Pharmaceuticals. It's repackaged: Major Pharmaceuticals rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-0710.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| West-Ward Columbus Inc. | Columbus, OH, United States | Makes it | No problems foundApr 30, 2026 · 27 inspections |
Recalls
- Dec 19, 2024 · Class III · West-Ward Columbus Inc
Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.
Lots: Lot # AC2556A; Exp. 03/2027
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Methadone: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA088109
- On the market since
- Jan 3, 2024
- Package NDCs
0904-7417-61- Official label
- DailyMed (National Library of Medicine), updated Jul 16, 2026
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