Package 60687-818-86

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-818-86
Digits Only 6068781886
Product NDC 60687-818
Product ID 60687-818_3506271d-27f4-2065-e063-6394a90ac386
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)

Marketing

Marketing Status
Marketed Since 2024-12-16
Brand methadone hydrochloride
Generic methadone hydrochloride
Sample Package No

Linked Drug Pages (1)

Methadone Hydrochloride ndc-match (0.95)

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"}