methadone hydrochloride

Generic: methadone hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methadone hydrochloride
Generic Name methadone hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methadone hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-1027
Product ID 63629-1027_c513c20b-ef58-4df1-8cce-ab397ef8e67c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090635
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2012-01-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 636291027
Hyphenated Format 63629-1027

Supplemental Identifiers

RxCUI
864706
UNII
229809935B

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 ANDA090635 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (63629-1027-1)
source: ndc

Packages (1)

63629-1027-1 100 TABLET in 1 BOTTLE (63629-1027-1)

Ingredients (1)

methadone hydrochloride (10 mg/1)

Linked Drug Pages (1)

METHADONE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c513c20b-ef58-4df1-8cce-ab397ef8e67c", "openfda": {"unii": ["229809935B"], "rxcui": ["864706"], "spl_set_id": ["3ce98ab4-346b-4680-b3e1-a8c29b3933af"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1027-1)", "package_ndc": "63629-1027-1", "marketing_start_date": "20200116"}], "brand_name": "METHADONE HYDROCHLORIDE", "product_id": "63629-1027_c513c20b-ef58-4df1-8cce-ab397ef8e67c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-1027", "dea_schedule": "CII", "generic_name": "METHADONE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHADONE HYDROCHLORIDE", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090635", "marketing_category": "ANDA", "marketing_start_date": "20120116", "listing_expiration_date": "20261231"}