17856-3554 NDC - METHADONE HYDROCHLORIDE ()

Drug Information

Product NDC: 17856-3554

Proprietary Name: Methadone Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ATLANTIC BIOLOGICALS CORP.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/13/2019

Package Information

No. Package Code Package Description Billing Unit
117856-3554-148 SYRINGE in 1 BOX, UNIT-DOSE (17856-3554-1) / 5 mL in 1 SYRINGE
217856-3554-248 SYRINGE in 1 BOX, UNIT-DOSE (17856-3554-2) / 5 mL in 1 SYRINGE
317856-3554-372 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-3554-3) / 10 mL in 1 CUP, UNIT-DOSE

NDC Record

Field Name Field Value Definition
PRODUCT NDC17856-3554The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEMethadone HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/13/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEATLANTIC BIOLOGICALS CORP.Name of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023