Package 13107-088-99

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 13107-088-99
Digits Only 1310708899
Product NDC 13107-088
Product ID 13107-088_73006026-6ba2-49da-824e-a4d05b99a2e7
Description

1000 TABLET in 1 BOTTLE (13107-088-99)

Marketing

Marketing Status
Marketed Since 2015-09-15
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": "73006026-6ba2-49da-824e-a4d05b99a2e7", "openfda": {"upc": ["0313107089015", "0313107088018"], "unii": ["229809935B"], "rxcui": ["864706", "864718"], "spl_set_id": ["6984eb5a-57a3-4686-bc67-91bc3e7a531e"], "manufacturer_name": ["Aurolife Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13107-088-01)", "package_ndc": "13107-088-01", "marketing_start_date": "20150915"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (13107-088-30)", "package_ndc": "13107-088-30", "marketing_start_date": "20150915"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (13107-088-99)", "package_ndc": "13107-088-99", "marketing_start_date": "20150915"}], "brand_name": "Methadone Hydrochloride", "product_id": "13107-088_73006026-6ba2-49da-824e-a4d05b99a2e7", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "13107-088", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "Aurolife Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203502", "marketing_category": "ANDA", "marketing_start_date": "20150915", "listing_expiration_date": "20261231"}