United States · FDA National Drug Code directory
METHADONE HYDROCHLORIDE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0054-0710_32014633-5c89-4163-9fa7-239777c04d1d
- Product NDC
- 0054-0710
- Form
- TABLET
- Composition / generic term
- METHADONE HYDROCHLORIDE
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19830308
- Source listing expiry
- 20271231
Source-listed ingredients
- METHADONE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (0054-0710-20) / 100 TABLET in 1 BLISTER PACK · 0054-0710-20
- 100 TABLET in 1 BOTTLE, PLASTIC (0054-0710-25) · 0054-0710-25
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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