methadone hydrochloride
Generic: methadone hydrochloride
Labeler: precision dose, inc.Drug Facts
Product Profile
Brand Name
methadone hydrochloride
Generic Name
methadone hydrochloride
Labeler
precision dose, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
methadone hydrochloride 5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68094-031
Product ID
68094-031_b9e6a3ca-9559-4dfa-b742-646be5def826
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA087393
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2020-12-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68094031
Hyphenated Format
68094-031
Supplemental Identifiers
RxCUI
UNII
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
ANDA087393 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/5mL
Packaging
- 3 TRAY in 1 CASE (68094-031-62) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (68094-031-59)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b9e6a3ca-9559-4dfa-b742-646be5def826", "openfda": {"unii": ["229809935B"], "rxcui": ["864761"], "spl_set_id": ["cbc42334-8783-4572-b8da-8c7451d14077"], "manufacturer_name": ["Precision Dose, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 TRAY in 1 CASE (68094-031-62) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (68094-031-59)", "package_ndc": "68094-031-62", "marketing_start_date": "20201223"}], "brand_name": "Methadone Hydrochloride", "product_id": "68094-031_b9e6a3ca-9559-4dfa-b742-646be5def826", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68094-031", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "Precision Dose, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA087393", "marketing_category": "ANDA", "marketing_start_date": "20201223", "listing_expiration_date": "20261231"}