NDC 17856-0392 – Methadone Hydrochloride

Methadone Hydrochloride 10 mg/mL · Concentrate · Oral

Human Prescription Drug DEA schedule CII

Product NDC17856-0392

Product details

Brand name
Methadone Hydrochloride
Generic name
Methadone Hydrochloride
Labeler
ATLANTIC BIOLOGICALS CORP.
Dosage form
Concentrate
Route
Oral
Marketing category
ANDA · ANDA040180
Marketed since
May 14, 2019
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
17856-0392-160 SYRINGE in 1 BOX, UNIT-DOSE (17856-0392-1) / .5 mL in 1 SYRINGEMay 20, 2024
17856-0392-372 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0392-3) / 2.5 mL in 1 CUP, UNIT-DOSE (17856-0392-4)May 20, 2024
17856-0392-61 SYRINGE in 1 BAG (17856-0392-6) / .5 mL in 1 SYRINGEMay 30, 2025
17856-0392-75 BOX, UNIT-DOSE in 1 SYRINGE (17856-0392-7) / 60 SYRINGE in 1 BOX, UNIT-DOSE (17856-0392-2) / 1 mL in 1 SYRINGE (17856-0392-5)May 20, 2024
17856-0392-81 SYRINGE in 1 BAG (17856-0392-8) / 1 mL in 1 SYRINGEMay 30, 2025
17856-0392-91 SYRINGE in 1 BAG (17856-0392-9) / 2.5 mL in 1 SYRINGEMay 30, 2025

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