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
- 81298-7500_57defc0a-f95c-43ed-bf34-8a53540d2a02
- Product NDC
- 81298-7500
- Form
- INJECTION
- Composition / generic term
- Methadone Hydrochloride
- Labeler
- Long Grove Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250628
- Source listing expiry
- 20271231
Source-listed ingredients
- METHADONE HYDROCHLORIDE — 200 mg/20mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, GLASS in 1 CARTON (81298-7500-1) / 20 mL in 1 VIAL, GLASS · 81298-7500-1
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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