Package 71610-455-09

Brand: tizanidine

Generic: tizanidine
NDC Package

Package Facts

Identity

Package NDC 71610-455-09
Digits Only 7161045509
Product NDC 71610-455
Description

9000 TABLET in 1 BOTTLE (71610-455-09)

Marketing

Marketing Status
Marketed Since 2020-08-25
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": "2c6a6719-33e4-44e8-bce6-30c10ae156a6", "openfda": {"unii": ["B53E3NMY5C"], "rxcui": ["313412"], "spl_set_id": ["d3b8d863-d13d-467c-97bf-5db9708036db"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "9000 TABLET in 1 BOTTLE (71610-455-09)", "package_ndc": "71610-455-09", "marketing_start_date": "20200825"}], "brand_name": "tizanidine", "product_id": "71610-455_2c6a6719-33e4-44e8-bce6-30c10ae156a6", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "71610-455", "generic_name": "tizanidine", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tizanidine", "active_ingredients": [{"name": "TIZANIDINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA076533", "marketing_category": "ANDA", "marketing_start_date": "20040116", "listing_expiration_date": "20261231"}