Package 72162-2560-1

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2560-1
Digits Only 7216225601
Product NDC 72162-2560
Description

100 TABLET in 1 BOTTLE (72162-2560-1)

Marketing

Marketing Status
Marketed Since 2025-11-04
Brand midodrine hydrochloride
Generic midodrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "94fb650d-3ad7-4447-b17e-c6ac262f27d0", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993466"], "spl_set_id": ["db4b18d6-68f9-4d7c-9230-40b928cf859c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2560-1)", "package_ndc": "72162-2560-1", "marketing_start_date": "20251104"}], "brand_name": "Midodrine Hydrochloride", "product_id": "72162-2560_94fb650d-3ad7-4447-b17e-c6ac262f27d0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "72162-2560", "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": "ANDA212774", "marketing_category": "ANDA", "marketing_start_date": "20200810", "listing_expiration_date": "20261231"}