Package 66689-836-99

Brand: methadone hydrochloride

Generic: methadone
NDC Package

Package Facts

Identity

Package NDC 66689-836-99
Digits Only 6668983699
Product NDC 66689-836
Product ID 66689-836_b76dbddc-b042-47d7-a7a7-f64c7c5c5035
Description

100 TABLET in 1 BOTTLE, PLASTIC (66689-836-99)

Marketing

Marketing Status
Marketed Since 2020-09-11
Brand methadone hydrochloride
Generic methadone
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": "b76dbddc-b042-47d7-a7a7-f64c7c5c5035", "openfda": {"unii": ["229809935B"], "rxcui": ["864706"], "spl_set_id": ["4a44bde6-c348-4316-b0e0-c24b407cb823"], "manufacturer_name": ["VistaPharm, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (66689-836-99)", "package_ndc": "66689-836-99", "marketing_start_date": "20200911"}], "brand_name": "Methadone Hydrochloride", "product_id": "66689-836_b76dbddc-b042-47d7-a7a7-f64c7c5c5035", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "66689-836", "dea_schedule": "CII", "generic_name": "Methadone", "labeler_name": "VistaPharm, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204166", "marketing_category": "ANDA", "marketing_start_date": "20200911", "listing_expiration_date": "20271231"}