Package 72241-043-07

Brand: tizanidine hydrochloride

Generic: tizanidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72241-043-07
Digits Only 7224104307
Product NDC 72241-043
Description

150 CAPSULE in 1 BOTTLE (72241-043-07)

Marketing

Marketing Status
Marketed Since 2017-12-29
Brand tizanidine hydrochloride
Generic tizanidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "92a36fc0-6663-404c-9a95-9e469527b143", "openfda": {"unii": ["B53E3NMY5C"], "rxcui": ["485484", "485485", "485486"], "spl_set_id": ["f8288ccd-6c66-415e-a06b-758971afe9a0"], "manufacturer_name": ["Modavar Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 CAPSULE in 1 BOTTLE (72241-043-07)", "package_ndc": "72241-043-07", "marketing_start_date": "20171229"}], "brand_name": "Tizanidine hydrochloride", "product_id": "72241-043_92a36fc0-6663-404c-9a95-9e469527b143", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "72241-043", "generic_name": "Tizanidine hydrochloride", "labeler_name": "Modavar Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tizanidine hydrochloride", "active_ingredients": [{"name": "TIZANIDINE HYDROCHLORIDE", "strength": "6 mg/1"}], "application_number": "ANDA210021", "marketing_category": "ANDA", "marketing_start_date": "20171229", "listing_expiration_date": "20261231"}