NDC 67877-659 – Methadone Hydrochloride

Methadone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC67877-659

Product details

Brand name
Methadone Hydrochloride
Generic name
Methadone Hydrochloride
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090635
Marketed since
July 1, 2025
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Methadone Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
67877-659-01100 TABLET in 1 BOTTLE (67877-659-01)Jul 1, 2025

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