NDC 71335-1360 – Methadone Hydrochloride

Methadone Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-1360

Product details

Brand name
Methadone Hydrochloride
Generic name
Methadone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090635
Marketed since
January 16, 2012
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-1360-0168 TABLET in 1 BOTTLE (71335-1360-0)Sep 28, 2022
71335-1360-115 TABLET in 1 BOTTLE (71335-1360-1)Sep 28, 2022
71335-1360-230 TABLET in 1 BOTTLE (71335-1360-2)Oct 1, 2019
71335-1360-390 TABLET in 1 BOTTLE (71335-1360-3)Aug 14, 2020
71335-1360-4120 TABLET in 1 BOTTLE (71335-1360-4)Sep 28, 2022
71335-1360-5180 TABLET in 1 BOTTLE (71335-1360-5)Sep 28, 2022
71335-1360-660 TABLET in 1 BOTTLE (71335-1360-6)Sep 28, 2022
71335-1360-728 TABLET in 1 BOTTLE (71335-1360-7)Sep 28, 2022
71335-1360-8112 TABLET in 1 BOTTLE (71335-1360-8)Sep 28, 2022
71335-1360-956 TABLET in 1 BOTTLE (71335-1360-9)Sep 28, 2022

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