methadone hydrochloride

Generic: methadone hydrochloride

Labeler: xlcare pharmaceuticals, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methadone hydrochloride
Generic Name methadone hydrochloride
Labeler xlcare pharmaceuticals, inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methadone hydrochloride 5 mg/1

Manufacturer
XLCare Pharmaceuticals, Inc

Identifiers & Regulatory

Product NDC 72865-120
Product ID 72865-120_639b24e8-927d-46ef-82f8-914a10528f21
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211228
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2019-01-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72865120
Hyphenated Format 72865-120

Supplemental Identifiers

RxCUI
864706 864718
UPC
0372865121016 0372865120019
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 ANDA211228 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72865-120-01)
source: ndc

Packages (1)

72865-120-01 100 TABLET in 1 BOTTLE (72865-120-01)

Ingredients (1)

methadone hydrochloride (5 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": "639b24e8-927d-46ef-82f8-914a10528f21", "openfda": {"upc": ["0372865121016", "0372865120019"], "unii": ["229809935B"], "rxcui": ["864706", "864718"], "spl_set_id": ["1a536622-dda3-41af-ab08-28e7c1bc9300"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72865-120-01)", "package_ndc": "72865-120-01", "marketing_start_date": "20190103"}], "brand_name": "Methadone Hydrochloride", "product_id": "72865-120_639b24e8-927d-46ef-82f8-914a10528f21", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72865-120", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "XLCare Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA211228", "marketing_category": "ANDA", "marketing_start_date": "20190103", "listing_expiration_date": "20261231"}