Package 57664-502-18

Brand: tizanidine

Generic: tizanidine
NDC Package

Package Facts

Identity

Package NDC 57664-502-18
Digits Only 5766450218
Product NDC 57664-502
Description

1000 TABLET in 1 BOTTLE (57664-502-18)

Marketing

Marketing Status
Marketed Since 2003-12-11
Brand tizanidine
Generic tizanidine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5e8ef5b3-9f58-46a7-833c-31ef018ea9a0", "openfda": {"unii": ["B53E3NMY5C"], "rxcui": ["313412", "313413"], "spl_set_id": ["4659df31-8b89-4eff-9d86-7b7e38de416b"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (57664-502-18)", "package_ndc": "57664-502-18", "marketing_start_date": "20031211"}, {"sample": false, "description": "150 TABLET in 1 BOTTLE (57664-502-89)", "package_ndc": "57664-502-89", "marketing_start_date": "20031211"}], "brand_name": "Tizanidine", "product_id": "57664-502_5e8ef5b3-9f58-46a7-833c-31ef018ea9a0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "57664-502", "generic_name": "Tizanidine", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tizanidine", "active_ingredients": [{"name": "TIZANIDINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA076416", "marketing_category": "ANDA", "marketing_start_date": "20031211", "listing_expiration_date": "20261231"}