Package 70518-3112-0

Brand: tizanidine

Generic: tizanidine
NDC Package

Package Facts

Identity

Package NDC 70518-3112-0
Digits Only 7051831120
Product NDC 70518-3112
Product ID 70518-3112_415e0425-9963-7244-e063-6294a90a9618
Description

60 TABLET in 1 BOTTLE, PLASTIC (70518-3112-0)

Marketing

Marketing Status
Marketed Since 2021-06-04
Brand tizanidine
Generic tizanidine
Sample Package No

Linked Drug Pages (1)

Tizanidine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "415e0425-9963-7244-e063-6294a90a9618", "openfda": {"unii": ["B53E3NMY5C"], "rxcui": ["313412"], "spl_set_id": ["7bbc81e5-ad3e-496b-908f-e6f500f6ad7e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-3112-0)", "package_ndc": "70518-3112-0", "marketing_start_date": "20210604"}], "brand_name": "Tizanidine", "product_id": "70518-3112_415e0425-9963-7244-e063-6294a90a9618", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70518-3112", "generic_name": "Tizanidine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tizanidine", "active_ingredients": [{"name": "TIZANIDINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA076286", "marketing_category": "ANDA", "marketing_start_date": "20210604", "listing_expiration_date": "20261231"}