Package 67296-2209-1

Brand: tizanidine

Generic: tizanidine
NDC Package

Package Facts

Identity

Package NDC 67296-2209-1
Digits Only 6729622091
Product NDC 67296-2209
Product ID 67296-2209_49add032-3efc-19f3-e063-6394a90a0d21
Description

21 TABLET in 1 BOTTLE, PLASTIC (67296-2209-1)

Marketing

Marketing Status
Marketed Since 2013-04-01
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": "49add032-3efc-19f3-e063-6394a90a0d21", "openfda": {"upc": ["0329300168150", "0329300169157"], "unii": ["B53E3NMY5C"], "rxcui": ["313412"], "spl_set_id": ["49adcfc8-3b1d-7f7e-e063-6294a90a361e"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (67296-2209-1)", "package_ndc": "67296-2209-1", "marketing_start_date": "20130401"}], "brand_name": "Tizanidine", "product_id": "67296-2209_49add032-3efc-19f3-e063-6394a90a0d21", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "67296-2209", "generic_name": "Tizanidine", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tizanidine", "active_ingredients": [{"name": "TIZANIDINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA091283", "marketing_category": "ANDA", "marketing_start_date": "20130401", "listing_expiration_date": "20271231"}