Package 72162-1517-1

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1517-1
Digits Only 7216215171
Product NDC 72162-1517
Product ID 72162-1517_c4296ad6-f454-4e6e-bf0b-2c1fc5d7271e
Description

100 TABLET in 1 BOTTLE (72162-1517-1)

Marketing

Marketing Status
Marketed Since 2023-10-06
Brand midodrine hydrochloride
Generic midodrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Midodrine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c4296ad6-f454-4e6e-bf0b-2c1fc5d7271e", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993466"], "spl_set_id": ["17b24a0b-03e4-4b58-87ab-3d66fec30226"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1517-1)", "package_ndc": "72162-1517-1", "marketing_start_date": "20231006"}], "brand_name": "Midodrine Hydrochloride", "product_id": "72162-1517_c4296ad6-f454-4e6e-bf0b-2c1fc5d7271e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "72162-1517", "generic_name": "Midodrine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA207169", "marketing_category": "ANDA", "marketing_start_date": "20181029", "listing_expiration_date": "20261231"}