Package 68071-3719-3

Brand: tizanidine

Generic: tizanidine
NDC Package

Package Facts

Identity

Package NDC 68071-3719-3
Digits Only 6807137193
Product NDC 68071-3719
Description

30 TABLET in 1 BOTTLE (68071-3719-3)

Marketing

Marketing Status
Marketed Since 2024-11-13
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": "2bae2620-0abb-7e55-e063-6394a90ad47c", "openfda": {"upc": ["0368071371932"], "unii": ["B53E3NMY5C"], "rxcui": ["313413"], "spl_set_id": ["26cffb1f-21a0-017f-e063-6394a90afb1a"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3719-3)", "package_ndc": "68071-3719-3", "marketing_start_date": "20241113"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3719-9)", "package_ndc": "68071-3719-9", "marketing_start_date": "20250114"}], "brand_name": "tizanidine", "product_id": "68071-3719_2bae2620-0abb-7e55-e063-6394a90ad47c", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "68071-3719", "generic_name": "tizanidine", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tizanidine", "active_ingredients": [{"name": "TIZANIDINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA208187", "marketing_category": "ANDA", "marketing_start_date": "20210304", "listing_expiration_date": "20261231"}