methadone hydrochloride

Generic: methadone hydrochloride

Labeler: vistapharm, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methadone hydrochloride
Generic Name methadone hydrochloride
Labeler vistapharm, llc
Dosage Form CONCENTRATE
Routes
ORAL
Active Ingredients

methadone hydrochloride 10 mg/mL

Manufacturer
VistaPharm, LLC

Identifiers & Regulatory

Product NDC 66689-694
Product ID 66689-694_a139d04a-25e0-499f-8bfb-43328f560410
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040088
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2009-10-30

Pharmacologic Class

Classes
full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 66689694
Hyphenated Format 66689-694

Supplemental Identifiers

RxCUI
991147
UNII
229809935B

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name methadone hydrochloride (source: ndc)
Generic Name methadone hydrochloride (source: ndc)
Application Number ANDA040088 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 1000 mL in 1 BOTTLE (66689-694-79)
  • 4000 mL in 1 BOTTLE (66689-694-88)
source: ndc

Packages (2)

Ingredients (1)

methadone hydrochloride (10 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a139d04a-25e0-499f-8bfb-43328f560410", "openfda": {"unii": ["229809935B"], "rxcui": ["991147"], "spl_set_id": ["d5bd3e97-b3f6-4bc2-9fb7-02921be35cdb"], "manufacturer_name": ["VistaPharm, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE (66689-694-79)", "package_ndc": "66689-694-79", "marketing_start_date": "20091030"}, {"sample": false, "description": "4000 mL in 1 BOTTLE (66689-694-88)", "package_ndc": "66689-694-88", "marketing_start_date": "20240819"}], "brand_name": "Methadone Hydrochloride", "product_id": "66689-694_a139d04a-25e0-499f-8bfb-43328f560410", "dosage_form": "CONCENTRATE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "66689-694", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "VistaPharm, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA040088", "marketing_category": "ANDA", "marketing_start_date": "20091030", "listing_expiration_date": "20271231"}