Package 66689-898-40

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 66689-898-40
Digits Only 6668989840
Product NDC 66689-898
Product ID 66689-898_9a8696a0-2dff-4277-a9a7-1a897f9a1860
Description

100 TABLET in 1 BOTTLE (66689-898-40)

Marketing

Marketing Status
Marketed Since 1998-03-25
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": "9a8696a0-2dff-4277-a9a7-1a897f9a1860", "openfda": {"upc": ["0366689898407"], "unii": ["229809935B"], "rxcui": ["864978"], "spl_set_id": ["c54baaee-8ea4-45f5-a5c8-bb84cf86832f"], "manufacturer_name": ["VistaPharm, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (66689-898-40)", "package_ndc": "66689-898-40", "marketing_start_date": "19980325"}], "brand_name": "Methadone Hydrochloride", "product_id": "66689-898_9a8696a0-2dff-4277-a9a7-1a897f9a1860", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "66689-898", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "VistaPharm, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA075082", "marketing_category": "ANDA", "marketing_start_date": "19980325", "listing_expiration_date": "20271231"}