Package 50090-5107-0

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-5107-0
Digits Only 5009051070
Product NDC 50090-5107
Product ID 50090-5107_b7fc852d-2c89-430e-81d2-c61614d4ccd7
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5107-0)

Marketing

Marketing Status
Marketed Since 2020-07-20
Brand tramadol hydrochloride
Generic tramadol hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b7fc852d-2c89-430e-81d2-c61614d4ccd7", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833709"], "spl_set_id": ["c28c98ac-7e07-46a5-8f34-57c008308fba"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5107-0)", "package_ndc": "50090-5107-0", "marketing_start_date": "20200720"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "50090-5107_b7fc852d-2c89-430e-81d2-c61614d4ccd7", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "50090-5107", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAMADOL HYDROCHLORIDE", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA200503", "marketing_category": "ANDA", "marketing_start_date": "20140819", "listing_expiration_date": "20261231"}