Package 16714-172-02

Brand: tizanidine

Generic: tizanidine
NDC Package

Package Facts

Identity

Package NDC 16714-172-02
Digits Only 1671417202
Product NDC 16714-172
Description

1000 TABLET in 1 BOTTLE (16714-172-02)

Marketing

Marketing Status
Marketed Since 2021-06-15
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": "a9995022-1f3f-f0dd-9672-60b074bfca01", "openfda": {"upc": ["0316714171012", "0316714172019"], "unii": ["B53E3NMY5C"], "rxcui": ["313412", "313413"], "spl_set_id": ["eed74219-9d4a-fecd-1bb9-ad6c01ad3e9d"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET in 1 BOTTLE (16714-172-01)", "package_ndc": "16714-172-01", "marketing_start_date": "20210615"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16714-172-02)", "package_ndc": "16714-172-02", "marketing_start_date": "20210615"}], "brand_name": "Tizanidine", "product_id": "16714-172_a9995022-1f3f-f0dd-9672-60b074bfca01", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "16714-172", "generic_name": "Tizanidine", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tizanidine", "active_ingredients": [{"name": "TIZANIDINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA076286", "marketing_category": "ANDA", "marketing_start_date": "20210615", "listing_expiration_date": "20261231"}