Package 70518-4248-0

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4248-0
Digits Only 7051842480
Product NDC 70518-4248
Product ID 70518-4248_4007fbf6-8ef0-85e9-e063-6394a90a4013
Description

30 TABLET in 1 BLISTER PACK (70518-4248-0)

Marketing

Marketing Status
Marketed Since 2024-12-30
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": "4007fbf6-8ef0-85e9-e063-6394a90a4013", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["c6104e62-5b2c-41a1-afb3-00dcf267a384"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4248-0)", "package_ndc": "70518-4248-0", "marketing_start_date": "20241230"}], "brand_name": "tramadol hydrochloride", "product_id": "70518-4248_4007fbf6-8ef0-85e9-e063-6394a90a4013", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "70518-4248", "dea_schedule": "CIV", "generic_name": "tramadol hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tramadol hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA202075", "marketing_category": "ANDA", "marketing_start_date": "20241230", "listing_expiration_date": "20261231"}