methadone hydrochloride

Generic: methadone hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methadone hydrochloride
Generic Name methadone hydrochloride
Labeler american health packaging
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

methadone hydrochloride 5 mg/5mL

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-818
Product ID 60687-818_3506271d-27f4-2065-e063-6394a90ac386
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA087393
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2024-12-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687818
Hyphenated Format 60687-818

Supplemental Identifiers

RxCUI
864761
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 ANDA087393 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 3 TRAY in 1 CASE (60687-818-86) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-818-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-818-40)
source: ndc

Packages (1)

60687-818-86 3 TRAY in 1 CASE (60687-818-86) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-818-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-818-40)

Ingredients (1)

methadone hydrochloride (5 mg/5mL)

Linked Drug Pages (1)

Methadone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3506271d-27f4-2065-e063-6394a90ac386", "openfda": {"unii": ["229809935B"], "rxcui": ["864761"], "spl_set_id": ["f935effe-e5b2-4bf7-bbde-6e80bb99076f"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TRAY in 1 CASE (60687-818-86)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-818-46)  / 5 mL in 1 CUP, UNIT-DOSE (60687-818-40)", "package_ndc": "60687-818-86", "marketing_start_date": "20241216"}], "brand_name": "Methadone Hydrochloride", "product_id": "60687-818_3506271d-27f4-2065-e063-6394a90ac386", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60687-818", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "American Health Packaging", "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": "20241216", "listing_expiration_date": "20261231"}