NDC 13107-089 – Methadone Hydrochloride

Methadone Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC13107-089

Product details

Brand name
Methadone Hydrochloride
Generic name
Methadone Hydrochloride
Labeler
Aurolife Pharma, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203502
Marketed since
September 15, 2015
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
13107-089-01100 TABLET in 1 BOTTLE (13107-089-01)Sep 15, 2015
13107-089-3030 TABLET in 1 BOTTLE (13107-089-30)Sep 15, 2015
13107-089-991000 TABLET in 1 BOTTLE (13107-089-99)Sep 15, 2015

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