Package 72789-327-20

Brand: tizanidine

Generic: tizanidine
NDC Package

Package Facts

Identity

Package NDC 72789-327-20
Digits Only 7278932720
Product NDC 72789-327
Product ID 72789-327_40bb3624-175c-7967-e063-6394a90af2dd
Description

20 TABLET in 1 BOTTLE, PLASTIC (72789-327-20)

Marketing

Marketing Status
Marketed Since 2023-06-12
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": "40bb3624-175c-7967-e063-6394a90af2dd", "openfda": {"upc": ["0372789327204"], "unii": ["B53E3NMY5C"], "rxcui": ["313413"], "spl_set_id": ["fdf4f09d-4537-a438-e053-6394a90a573d"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (72789-327-20)", "package_ndc": "72789-327-20", "marketing_start_date": "20230612"}], "brand_name": "Tizanidine", "product_id": "72789-327_40bb3624-175c-7967-e063-6394a90af2dd", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "72789-327", "generic_name": "Tizanidine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tizanidine", "active_ingredients": [{"name": "TIZANIDINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA076416", "marketing_category": "ANDA", "marketing_start_date": "20031211", "listing_expiration_date": "20261231"}