Package 70518-0942-0

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-0942-0
Digits Only 7051809420
Product NDC 70518-0942
Product ID 70518-0942_48485d0d-d2e9-2271-e063-6294a90af571
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-0942-0)

Marketing

Marketing Status
Marketed Since 2018-01-09
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": "48485d0d-d2e9-2271-e063-6294a90af571", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833709"], "spl_set_id": ["16053b28-c759-4914-93e6-2de0afe72445"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-0942-0)", "package_ndc": "70518-0942-0", "marketing_start_date": "20180109"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-0942-2)", "package_ndc": "70518-0942-2", "marketing_start_date": "20240710"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "70518-0942_48485d0d-d2e9-2271-e063-6294a90af571", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "70518-0942", "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": "100 mg/1"}], "application_number": "ANDA200503", "marketing_category": "ANDA", "marketing_start_date": "20180109", "listing_expiration_date": "20271231"}