methadone hydrochloride
Generic: methadone hydrochloride
Labeler: vistapharm, llcDrug Facts
Product Profile
Brand Name
methadone hydrochloride
Generic Name
methadone hydrochloride
Labeler
vistapharm, llc
Dosage Form
CONCENTRATE
Routes
Active Ingredients
methadone hydrochloride 10 mg/mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
66689694
Hyphenated Format
66689-694
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 1000 mL in 1 BOTTLE (66689-694-79)
- 4000 mL in 1 BOTTLE (66689-694-88)
Packages (2)
Ingredients (1)
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"}