Package 0406-0527-10
Brand: methadose
Generic: methadone hydrochloridePackage Facts
Identity
Package NDC
0406-0527-10
Digits Only
0406052710
Product NDC
0406-0527
Description
1000 mL in 1 BOTTLE, PLASTIC (0406-0527-10)
Marketing
Marketing Status
Brand
methadose
Generic
methadone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1d37bef9-02d8-4da4-b01e-6eec35380ed6", "openfda": {"upc": ["0304068725104", "0304060527102"], "unii": ["229809935B"], "rxcui": ["991147", "991149"], "spl_set_id": ["808a9d0b-720b-4034-a862-5122ff514608"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (0406-0527-10)", "package_ndc": "0406-0527-10", "marketing_start_date": "19730314"}], "brand_name": "METHADOSE", "product_id": "0406-0527_1d37bef9-02d8-4da4-b01e-6eec35380ed6", "dosage_form": "CONCENTRATE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0406-0527", "dea_schedule": "CII", "generic_name": "methadone hydrochloride", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHADOSE", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "NDA017116", "marketing_category": "NDA", "marketing_start_date": "19730314", "listing_expiration_date": "20261231"}