Package 31722-947-01

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 31722-947-01
Digits Only 3172294701
Product NDC 31722-947
Product ID 31722-947_24878a39-232d-45f6-af1f-fbb00eb5d915
Description

100 TABLET in 1 BOTTLE (31722-947-01)

Marketing

Marketing Status
Marketed Since 2019-01-03
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": "24878a39-232d-45f6-af1f-fbb00eb5d915", "openfda": {"upc": ["0331722947015", "0331722946018"], "unii": ["229809935B"], "rxcui": ["864706", "864718"], "spl_set_id": ["8f4cf84e-165c-489d-a668-0f715053f196"], "manufacturer_name": ["Camber Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-947-01)", "package_ndc": "31722-947-01", "marketing_start_date": "20190103"}], "brand_name": "Methadone Hydrochloride", "product_id": "31722-947_24878a39-232d-45f6-af1f-fbb00eb5d915", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "31722-947", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA211228", "marketing_category": "ANDA", "marketing_start_date": "20190103", "listing_expiration_date": "20261231"}