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 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0493
Product ID 71335-0493_eb6232eb-a7e6-40ae-ada5-54ca950c9e17
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203502
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2015-09-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350493
Hyphenated Format 71335-0493

Supplemental Identifiers

RxCUI
864718
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 ANDA203502 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (71335-0493-1)
  • 30 TABLET in 1 BOTTLE (71335-0493-2)
  • 120 TABLET in 1 BOTTLE (71335-0493-3)
  • 112 TABLET in 1 BOTTLE (71335-0493-4)
  • 60 TABLET in 1 BOTTLE (71335-0493-5)
  • 180 TABLET in 1 BOTTLE (71335-0493-6)
  • 28 TABLET in 1 BOTTLE (71335-0493-7)
source: ndc

Packages (7)

Ingredients (1)

methadone hydrochloride (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eb6232eb-a7e6-40ae-ada5-54ca950c9e17", "openfda": {"unii": ["229809935B"], "rxcui": ["864718"], "spl_set_id": ["cc79daec-2430-4d17-a37d-5a7ff5bfd883"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0493-1)", "package_ndc": "71335-0493-1", "marketing_start_date": "20180316"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0493-2)", "package_ndc": "71335-0493-2", "marketing_start_date": "20180827"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0493-3)", "package_ndc": "71335-0493-3", "marketing_start_date": "20240809"}, {"sample": false, "description": "112 TABLET in 1 BOTTLE (71335-0493-4)", "package_ndc": "71335-0493-4", "marketing_start_date": "20240809"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0493-5)", "package_ndc": "71335-0493-5", "marketing_start_date": "20240809"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-0493-6)", "package_ndc": "71335-0493-6", "marketing_start_date": "20240809"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-0493-7)", "package_ndc": "71335-0493-7", "marketing_start_date": "20240809"}], "brand_name": "Methadone Hydrochloride", "product_id": "71335-0493_eb6232eb-a7e6-40ae-ada5-54ca950c9e17", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-0493", "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": "5 mg/1"}], "application_number": "ANDA203502", "marketing_category": "ANDA", "marketing_start_date": "20150915", "listing_expiration_date": "20261231"}